Substituted pyrazolo[1,5-a][1,3,5]triazines as CDK inhibitors

[0001] This application is a Continuation-in-Part of U.S. application Ser. No. 17/045,009, filed Oct. 2, 2020; which is a National Stage Application of International Application Number PCT/EP2019/059289, filed Apr. 11, 2019; which claims the benefit of U.S. Provisional Application Ser. No. 62/656,041, filed Apr. 11, 2018, in their entirety.

[0002] The present invention relates to pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof, the use of these derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferative diseases, inflammatory diseases, immunological diseases, cardiovascular diseases and infectious diseases. Furthermore, the present invention is directed towards pharmaceutical compositions containing at least one of the pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof.

[0003] Cyclin-dependent kinase (CDK) family members that trigger passage through the cell cycle are being considered as attractive therapeutic targets, especially for cancer. CDK family members that control other processes such as transcription and RNA processing have caught less attention so far, although experimental evidence for their involvement in different pathological processes is emerging. Together with cell cycle control, CDK/cyclin complexes also have been identified as conserved components of the RNA polymerase II (Pol II) transcriptional machinery (Bregman et al., 2000, Front Biosci. 5:244-257). There are currently 20 known mammalian CDKs. While CDK7-13 have been linked to transcription, only CDK 1, 2, 4, and 6 show demonstrable association with cell cycle. Unique among the mammalian CDKs, CDK7 has consolidated kinase activities, regulating both the cell cycle progression and transcription (Desai et al., 1995, Mol. Cell Biol. 15, 345-350).

[0004] The general transcription factor TFIIH purified from mammalian cells consists of ten subunits, seven of which (p62, p52, p44, p34, XPD, XPB, and TTDA) form the core complex. Three subunits (cyclin H, MAT1, and CDK7) from the CDK-activating kinase (CAK), which is linked to TFIIH's core via the XPD (ATP-dependent helicase) subunit of complex. During the process of transcription initiation, the helicase activity of TFIIH opens the core promoter DNA, while CDK7 phosphorylates the C-terminal domain (CTD) of Pol II at serine 5 and 7 (Akhtar et al., 2009, Mol. Cell 34, 387-393) as well as other transcription factors controlling the initiation-to-elongation transition (Larochelle et al., 2012, Nat. Strut. Mol. Biol. 19, 1108-1115 Therefore CDK7 is essential factor for transcription process, which suggests that CDK7 is a target for cancer therapy, especially transcription addicted cancer.

[0005] CDK7 has long been asserted as having an essential role in cellular metabolism and viability. Transcriptional CDK inhibitors down-regulate a large number of short-lived anti-apoptotic proteins, such as the anti-apoptotic proteins myeloid cell leukemia-1 (Mcl-1), B-cell lymphoma extra-long (Bcl-xL) and XIAP (X-linked IAP), D-cyclins, c-Myc, Mdm-2 (leading to p53 stabilization), p21^waf1 proteins whose transcription is mediated by nuclear factor-kappa B (NF-kB) and hypoxia-induced VEGF (Shapiro G I. 2006, J Clin Oncol; 24(11):1770-83). The transcriptional non-selective cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in multiple myeloma cells through transcriptional repression and down-regulation of Mcl-1. These findings supported previous postulates that CDK7 might be a valuable target for drugs directed toward the treatment of malignancies and cell cycle-associated diseases (Lolli G and Johnson L N. 2005. Cell Cycle 4:572-577).

[0006] The function of CDK7 as regulator of general transcription and CDK7 is a therapeutic target for treatment of many diseases and syndromes are associated with mutations in regulatory regions and in transcription factors, cofactors, chromatin regulators and noncoding RNAs. These mutations can contribute to cancer, autoimmunity, neurological disorders, developmental syndromes, diabetes, cardiovascular disease, and obesity, among others. Some transcription factors control RNA polymerase II pause release and elongation and, when their expression or function is altered, can produce aggressive tumor cells (c-Myc) or some forms of autoimmunity (AIRE) (Tong Ihn Lee and Richard A. Young, Cell, 2013, 152:1237-1251). Therefore, inhibition of human CDK7 kinase activity is likely to result in anti-proliferative activity through the function in cell cycle progression and transcriptional regulation by inhibition of some transcription factor related to oncogene through inhibition of general transcription process. More important thing is that CDK7 has been shown to regulate exponential expression of oncogenic transcription factors more dramatically than it does to other housekeeping genes in cancer cells. Thus Inhibition of CDK7 can differentially affect transcription of certain oncogenes and housekeeping gene, therefore therapeutic window can be secured. For this reason, transcriptional regulation and pharmacological inhibition through appropriate general transcription inhibition by CDK7 could be applied to treat proliferative disorder, including cancer. As a general regulator of transcription, CDK7 is a therapeutic target for treatment of disease like inflammation, virus replication such as HIV, EBV, cancer and cardiac hypertrophy.

[0007] HIV-1 gene expression is regulatory by a viral transactivator protein (Tat) which induces transcriptional elongation of HIV-1 long tandem repeat. This induction requires hyperphosphorylation of the C-terminal domain repeat of RNA polymerase II. To archives said hyperphosphorylation, Tat stimulates CTD kinases associated with general transcription factors of the promoter complex, specifically TFIIH-associated CDK7 (Nekhai et al.; Biochem J. (2002) 364, 649-657). The inventors of US 615968 also described that Tat binds to CDK7 and that this interaction increase the ability of CAK to phosphorylate CTD. The authors of US 615968 further disclose that the transcriptional activation by Tat is dependent upon the kinase activity of CDK7. Additionally, Young Kyeung Kim and colleagues conclude that the recruitment and activation of TFIIH represents a rate-limiting step for the emergence of HIV from latency (Young Kyeung Kim, EMBO (2006) 25, 3596-3604).

[0008] Levels of CDK7 and CDK9, as well as other components of the kinase complexes, MAT-1/cyclin H are upregulated during Human cytomegalovirus infection. In addition, there is an increase in the kinase activities of CDK7 and CDK9 (Tamrakar et al., Journal of Virology, 2005, 79; 15477-15493).

[0009] Many antiviral drugs target viral proteins. These have the disadvantage that viruses often develop resistance against these drugs. Antiviral drugs targeting cellular proteins essential for viral process, like CDK7, could bypass this disadvantage. These drugs may further be effective in treating several unrelated viruses and their effects should be additive to traditional antiviral agents. Inhibitors of CDK7, which has its dual function of CDK-activating kinase and transcription regulation is very effective in the treatment of several viruses.

[0010] It is an object of the present invention to provide compounds and/or pharmaceutically acceptable salts thereof which can be used as pharmaceutically active agents, especially for prophylaxis and/or treatment of cell proliferative diseases, inflammatory diseases, immunological diseases, cardiovascular diseases and infectious diseases, as well as compositions comprising at least one of those compounds and/or pharmaceutically acceptable salts thereof as pharmaceutically active ingredients.

[0011] In one aspect, the present invention relates to pyrazolo-triazine or pyrazolo-pyrimidine compounds which are defined by general formula I

[0012]
wherein

• • [0013] X is, independently at each occurrence, selected from CH and N;
  • [0014] Q is either absent or independently, at each occurrence, selected from the group consisting of —NH—, —NH(CH₂)—, —NH(CH₂)₂—, —NH(C═O)—, —NHSO₂—, —O—, —O(CH₂)—, —(C═O)—, —(C═O)NH— and —(C═O)(CH₂)—;
  • [0015] Y is, independently at each occurrence, selected from the group consisting of halogen, C1-C3 haloalkyl, C3-C8 cycloalkyl, aryl, heteroaryl, heterocyclyl, —S(═O)₂R³, C1-C6 alkyl and C1-C6 alkyl substituted with one or two of —OR⁵, —N(R⁵)R⁵, aryl, heteroaryl and heterocyclyl;
  • [0016] Wherein C3-C8 cycloalkyl is optionally substituted with one or two of R³, R⁴ and —(C═O)R⁵, wherein heterocyclyl is optionally substituted with one or two of R³, R⁴ and —(C═O)R⁵, and wherein aryl or heteroaryl is optionally substituted with one or two of R³, C1-C6 alkyl, —OR⁵, —N(R⁵)R⁵, —(C═O)R⁵, halogen, heteroaryl and heterocyclyl;
  • [0017] R¹ is, at each occurrence, independently selected from the group consisting of hydrogen and methyl;
  • [0018] R² is, at each occurrence, independently selected from the group consisting of halogen, C1-C6 alkyl, C3-C10 cycloalkyl, —CN, —(C═O)CH₃ and C1-C3 haloalkyl, any of which is optionally substituted;
  • [0019] R³ is either absent or independently, at each occurrence, selected from the group consisting of hydrogen, —OR⁵, halogen, C1-C3 haloalkyl, —CN, —N(R⁵)R⁵, (═O), —NH(C═O)R⁵, —(C═O)NH₂, —S(═O)₂N(R⁵)R⁵, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OR₅, —NH₂ or —S(═O)₂N(R⁵)R⁵;
  • [0020] R⁴ is, independently, at each occurrence, selected from the group consisting of hydrogen, halogen, C1-C3 haloalkyl, —CN, —OR⁵, —N(R⁵)R⁵, (═O), S(═O)₂N(R⁵)R⁵, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OH, —NH₂ or —S(═O)₂N(R⁵)R⁵;
  • [0021] wherein both R³ and R⁴ are (═O) if attached to a single sulfur atom that forms part of Y being a heterocycle;
  • [0022] or wherein R³ and R⁴, together with the structure to which they are attached, form an aromatic ring, a heteroaromatic ring, a saturated or unsaturated heterocyclic ring, or a fused or bridged ring structure of any of an aromatic ring, a heteroaromatic ring, and a saturated or unsaturated heterocyclic ring;
  • [0023] R⁵ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, heteroaryl, heterocyclyl, heteroaryl substituted with one or two of halogen, —OR¹¹, —N(R¹¹)R¹¹, C1-C6 alkyl and C1-C6 alkyl substituted with —OH, —NH₂; heterocyclyl substituted with one or two of halogen, —OR¹¹, —N(R¹¹)R¹¹, C1-C6 alkyl and C1-C6 alkyl substituted with —OH or —NH₂;
  • [0024] Z is any structure of the following group A;

[0025]

• • [0026] Wherein n=1, 2, or 3; m=1, or 2;
  • [0027] R⁶ and R⁷ are, at each occurrence, independently selected from the group consisting of hydrogen, —NH(C═O)R¹⁴, —NHR¹⁴, —OR¹⁴ and any structure of the following group B, with the proviso that, when Z is

[0028]

• • [0029]  one of R⁶ and R⁷ is not H;

[0030]

• • [0031] wherein o is, independently at each occurrence, selected from 1, 2 and 3;
  • [0032] W is any structure of the following group C;

[0033]

• • [0034] L is absent or, at each occurrence, independently selected from the group consisting of —O— and —NH—;
  • [0035] wherein n is, independently at each occurrence, selected from 1, 2 and 3;
  • [0036] R⁸, R⁹ and R¹⁰ are, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —CN and C1-C6 alkyl substituted with —OH, —OR⁵ or —NHR⁵;
  • [0037] R¹¹ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C10 cycloalkyl and W, as defined above;
  • [0038] R¹² is, at each occurrence, independently selected from hydrogen and W, as defined above;
  • [0039] Wherein if R¹¹ is W, R¹² is hydrogen;
  • [0040] R¹³ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵, —CN and W, as defined above;
  • [0041] Wherein if R¹³ is W, R¹² is hydrogen;
  • [0042] R¹⁴ is any structure of group D;

[0043]

• • [0044] R¹⁵ is, at each occurrence, independently selected from hydrogen and W, as defined above;
  • [0045] R¹⁶ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵, —CN and W, as defined above;
  • [0046] Wherein if R¹⁶ is W, R¹² is hydrogen;
  • [0047] R¹⁷ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl and C1-C3 haloalkyl;
  • [0048] R¹⁸ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵ and —CN;
  • [0049] R¹⁹ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C10 cycloalkyl and W, as defined above;
  • [0050] Wherein if R¹⁹ is W, R¹⁵ is hydrogen;
  • [0051] R²⁰ and R²¹ are, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —OR⁵, heterocyclyl and —CN;
  • [0052] R²² is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C3-C10 cycloalkyl, —N(R⁵)₂, —NR¹⁹R²⁰, —NR¹⁹CH₂(CO)NH₂, heterocyclyl, —OR⁵ and —CN;
  • [0053] or an enantiomer, stereoisomeric form, mixture of enantiomers, diastereomer, mixture of diastereomers, racemate of the above mentioned compounds or a pharmaceutically acceptable salt thereof.

[0054] It should be noted that the present invention also relates to enantiomers, stereoisomeric forms, mixtures of enantiomers, diastereomers, mixtures of diastereomers, racemates of the compounds mentioned herein and to pharmaceutically acceptable salts thereof.

[0055] In one embodiment of the compounds of general formula I, the compounds have the general formula Ia

[0056]
wherein

• • [0057] X is, independently at each occurrence, selected from CH and N;
  • [0058] Y¹ is, independently at each occurrence, selected from CH, C(OH) and N;
  • [0059] Y² is, independently at each occurrence, selected from CH, C(OH) and N;
  • [0060] Q is absent or, at each occurrence, independently selected from the group consisting of —NH—, —NH(CH₂)—, —NH(C═O)—, —NHSO₂—, —O—, —O(CH₂)—, —(C═O)— and —(C═O)(CH₂)—;
  • [0061] R¹ is, at each occurrence, independently selected from the group consisting of hydrogen and methyl;
  • [0062] R² is, at each occurrence, independently selected from the group consisting of halogen, C1-C6 alkyl, C3-C10 cycloalkyl, —CN, —(C═O)CH₃ and C1-C3 haloalkyl, any of which is optionally substituted;
  • [0063] R³ is either absent or independently, at each occurrence, selected from the group consisting of hydrogen, —OR⁵, halogen, C1-C3 haloalkyl, —CN, —N(R⁵)R⁵, (═O), —NH(C═O)R⁵, —(C═O)NH₂, —S(═O)₂N(R⁵)R⁵, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OR₅, —NH₂ or —S(═O)₂N(R⁵)R⁵;
  • [0064] R⁴ is, independently, at each occurrence, selected from the group consisting of hydrogen, halogen, C1-C3 haloalkyl, —CN, —N(R⁵)R⁵, (═O), S(═O)₂N(R⁵)R⁵, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OH, —NH₂ or —S(═O)₂N(R⁵)R⁵;
  • [0065] wherein both R³ and R⁴ are (═O) if attached to a single sulfur atom that forms part of Y being a heterocycle;
  • [0066] or wherein R³ and R⁴, together with the structure to which they are attached, form an aromatic ring, a heteroaromatic ring, a saturated or unsaturated heterocyclic ring, or a fused or bridged ring structure of any of an aromatic ring, a heteroaromatic ring, and a saturated or unsaturated heterocyclic ring;
  • [0067] R⁵ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, heteroaryl, heterocyclyl, heteroaryl substituted with one or two of halogen, —OR¹¹, —N(R¹¹)R¹¹, C1-C6 alkyl and C1-C6 alkyl substituted with —OH, —NH₂; heterocyclyl substituted with one or two of halogen, —OR¹¹, —N(R¹¹)R¹¹), C1-C6 alkyl and C1-C6 alkyl substituted with —OH or —NH₂;
  • [0068] Z is any structure of the following group A;

[0069]

• • [0070] wherein n=1, 2, or 3; m=1, or 2;
  • [0071] R⁶ and R⁷ are, at each occurrence, independently selected from the group consisting of hydrogen, —NH(C═O)R¹⁴, —NHR¹⁴, —OR¹⁴ and any structure of the following group B, with the proviso that, when Z is

[0072]

• • [0073]  one of R6 and R7 is not H;

[0074]

• • [0075] wherein o=1, 2 or 3;
  • [0076] W is any structure of the following group C;

[0077]

• • [0078] L is absent or, at each occurrence, independently selected from the group consisting of —O— and —NH—;
  • [0079] R⁸, R⁹ and R¹⁰ are, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —OR⁵, —CN and C1-C6 alkyl substituted with —OH, —OR⁵ or —NHR⁵;
  • [0080] R¹¹ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C10 cycloalkyl and W, as defined above;
  • [0081] R¹² is, at each occurrence, independently selected from hydrogen and W, as defined above;
    • [0082] wherein if R¹¹ is W, R¹² is hydrogen;
  • [0083] R¹³ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵, —CN and W, as defined above;
    • [0084] wherein if R¹³ is W, R¹² is hydrogen;
  • [0085] R¹⁴ is any structure of group D;

[0086]

• • [0087] R¹⁵ is, at each occurrence, independently selected from hydrogen and W, as defined above;
  • [0088] R¹⁶ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵, —CN and W, as defined above;
    • [0089] wherein if R¹⁶ is W, R¹² is hydrogen;
  • [0090] R¹⁷ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl and C1-C3 haloalkyl;
  • [0091] R¹⁸ is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, —NH₂, —OR⁵ and —CN;
  • [0092] R¹⁹ is, at each occurrence, independently selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C10 cycloalkyl and W, as defined above;
    • [0093] wherein if R¹⁹ is W, R¹⁵ is hydrogen;
  • [0094] R²⁰ and R²¹ are, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C3 haloalkyl, heterocyclyl and —CN;
  • [0095] R²² is, at each occurrence, independently selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C3-C10 cycloalkyl, —N(R⁵)₂, —NR¹⁹R²⁰, heterocyclyl, —OR⁵ and —CN.

[0096] In one embodiment of the compounds of general formula I or formula Ia above, at least one of Z, R⁶, R⁷, R¹¹, R¹², R¹³, R¹⁵, R¹⁶ and R¹⁹ is W, as defined above for formula I or formula Ia, or is a structure containing W, as defined above for formula I or formula Ia.

[0097] In one embodiment of the compounds of general formula I or formula Ia above, exactly one of Z, R⁶, R⁷, R¹¹, R¹², R¹³, R¹⁵, R¹⁶ and R¹⁹ is W, as defined above for formula I or formula Ia, or is a structure containing W, as defined above for formula I or formula Ia.

[0098] In one embodiment of the compounds of general formula I above, R′ is hydrogen and the compound has the general formula II

[0099]

• • [0100] wherein X, Y, Z, R² and Q are as defined for general formula I.

[0101] In one embodiment of the compounds of general formula I above, the compounds have the general formula III

[0102]

• • [0103] wherein X, Z, R² and Q are as defined above for general formula I, and
  • [0104] Y^a is either absent or independently, at each occurrence, selected from the group consisting of aryl, heteroaryl, heterocyclyl, aryl substituted with one or two of C1-C6 alkyl, —OR⁵, —N(R⁵)R⁵, and halogen, heteroaryl substituted with one or two of C1-C6 alkyl, —OR⁵, —N(R⁵)R⁵ and halogen, heterocyclyl substituted with one or two of R²³ and R²⁴;
  • [0105] R²³ is either absent or independently, at each occurrence, selected from the group consisting of hydrogen, —OR⁵, halogen, —N(R⁵)R⁵, —NH(C═O)R⁵, —(C═O)NH₂, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OH or —NH₂;
  • [0106] R²⁴ is, independently, at each occurrence, selected from the group consisting of hydrogen, halogen, —OR⁵, —N(R⁵)R⁵, (═O), aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OH or —NH₂;
  • [0107] wherein R⁵ is as defined above for formula I;
  • [0108] L¹ is either absent or independently, at each occurrence, selected from the group consisting of —NH—, —NH(CH₂)—, —NH(C═O)—, —NHSO₂—, —O—, —O(CH₂)—, —(C═O)—, —(C═O)NH— and —(C═O)(CH₂)—;
  • [0109] Y¹ is, independently at each occurrence, selected from CH, C(OH) and N;
  • [0110] Y² is, independently at each occurrence, selected from CH, C(OH), O and N;
  • [0111] q is, independently at each occurrence, selected from 0, 1 and 2;
  • [0112] r is, independently at each occurrence, selected from 0, 1, 2 and 3;

[0113] In one embodiment of the compounds of general formula I or general formula Ia above, Z is Z¹, and Z¹ is any structure of the following group E;

[0114]

• • [0115] wherein m is, independently at each occurrence, selected from 1 and 2; and
  • [0116] n is as defined above for general formula I;
  • [0117] R⁸, R⁹, R¹² and R¹³ are as defined for general formula I;
  • [0118] R⁶ is any structure of group B as defined for general formula I.

[0119] In one embodiment of the compounds of general formula I or general formula Ia above, Z is

[0120]

• • [0121] p is, independently at each occurrence, selected from 0, 1, 2 and 3;
  • [0122] X¹ is, independently at each occurrence, selected from CR⁸ and N;
  • [0123] R⁶ is any structure of group B, as defined in above for general formula I; and
  • [0124] R⁸ is as defined above for general formula I.

[0125] In one embodiment of the compounds of general formula I or general formula Ia above,

• • [0126] Z is

[0127]

• • [0128] or Z is

[0129]

• • [0130] wherein R⁶-R⁸ are as defined above for general formula I.

[0131] In one embodiment of the compounds of general formula I or general formula Ia above,

• • [0132] Z is

[0133]

• • [0134] wherein R⁶ and R¹⁰ are as defined above for general formula I.

[0135] In one embodiment of the compounds of general formula I or general formula Ia above, the compounds have the general formula IV

[0136]

• • [0137] wherein X, X¹, R⁶, R⁸ and Q are as defined above for general formula I, and
  • [0138] X¹ is as defined above;
  • [0139] wherein Y^b is any structure of the following group F;

[0140]

• • [0141] R²⁶ and R²² is either absent or independently, at each occurrence, selected from the group consisting of hydrogen, —OR⁵, halogen, —N(R⁵)R⁵, —NH(C═O)R⁵, —(C═O)NH₂, aryl, heteroaryl, heterocyclyl, C1-C6 alkyl and C1-C6 alkyl substituted with —OH or —NH₂;
  • [0142] wherein R⁵ is as defined above for general formula I.

[0143] In one embodiment of the compounds of general formula I or general formula Ia above, R² is C1-C6 alkyl or C1-C3 haloalkyl.

[0144] In one embodiment of the compounds of general formula I or general formula Ia above, R⁶ is

[0145]

[0146] In one embodiment of the compounds of general formula I above or of general formula Ia above,

• • [0147] R⁶ and R⁷ are, at each occurrence, independently selected from —NH(C═O)R¹⁴, —NHR¹⁴, —OR¹⁴, any structure of the following group B′

[0148]

• • [0149] wherein R¹⁴ is selected from the group consisting of

[0150]

• • [0151] wherein R⁵, R⁸, R¹², R¹⁶, R¹⁷, R¹⁸ and W are as defined herein.

[0152] In one embodiment of the compounds of general formula I above or of general formula Ia above, W is selected from the group consisting of

[0153]

• • [0154] R²⁰-R²² and L being as defined herein.

[0155] In one embodiment of the compounds of general formula Ia above or of general formula III above, Y¹ is N, Y² is CH, and R³ is —N(R⁵)₂, R⁵ being as defined herein.

[0156] In one embodiment, the present invention also relates to pharmaceutically acceptable salts of the compounds according to the present invention, as defined herein.

[0157] In one embodiment of the compounds of general formula I or general formula Ia above, the compounds have a structure selected from structures 1-216, as defined in table 7.

[0158] In a preferred embodiment, the compounds have a structure selected from compounds 11, 31, 32, 34, 36, 44, 46, 48, 51, 52, 54, 59, 61, 64, 67, 79, 80, 82, 94, 95, 116, 118, 120, 123, 128, 137, 147, 150, 151, 153, 158, 160, 161, 163, 164, 171-181, 184-188, 190, 203 and 204.

[0159] In a further aspect, the present invention also relates to a pharmaceutical composition comprising a compound according to the present invention, as defined herein, as an active ingredient, together with at least one pharmaceutically acceptable carrier, excipient and/or diluent.

[0160] In one aspect, the present invention also relates to a compound according to the present invention as defined herein, for use as a pharmaceutical or pharmaceutically active agent, wherein said pharmaceutical or pharmaceutically active agent preferably has an inhibitory activity on cyclin-dependent kinase 7 (CDK7).

[0161] In one aspect, the present invention also relates to a compound according to the present invention, as defined herein, for use in a method of prevention and/or treatment of a disease which is associated with inhibition of apoptosis, abnormal transcriptional activity and/or cell cycle arrest by aberrant activity and/or overexpression of one or several cyclin-dependent kinases (CDKs), in particular cyclin-dependent kinase 7 (CDK7), wherein the disease is selected from proliferative diseases, infectious diseases, including opportunistic diseases, immunological diseases, autoimmune diseases, and inflammatory diseases, such diseases being as defined herein.

[0162] In a further aspect, the present invention also relates to a method of prevention and/or treatment of a disease which is associated with inhibition of apoptosis, abnormal transcriptional activity and/or cell cycle arrest by aberrant activity and/or overexpression of one or several cyclin-dependent kinases (CDKs), in particular cyclin-dependent kinase 7 (CDK7), wherein the disease is selected from proliferative diseases, infectious diseases, including opportunistic diseases, immunological diseases, autoimmune diseases, and inflammatory diseases; wherein the method comprises administering to a subject in need of such prevention and/or treatment a compound according to the present invention as defined herein.

[0163] In one embodiment, the proliferative disease is a cancer, preferably a cancer selected from the group comprising or consisting of: adenocarcinoma, choroidal melanoma, acute leukemia, acoustic neurinoma, ampullary carcinoma, anal carcinoma, astrocytoma, basal cell carcinoma, pancreatic cancer, Desmoid tumor, bladder cancer, bronchial carcinoma, estrogen dependent and independent breast cancer, Burkitt's lymphoma, corpus cancer, Carcinoma unknown primary tumor (CUP-syndrome), colorectal cancer, small intestine cancer, small intestinal tumors, ovarian cancer, endometrial carcinoma, ependymoma, epithelial cancer types, Ewing's tumors, gastrointestinal tumors, gastric cancer, gallbladder cancer, gall bladder carcinomas, uterine cancer, cervical cancer, cervix, glioblastomas, gynecologic tumors, ear, nose and throat tumors, hematologic tumor, hairy cell leukemia, urethral cancer, skin cancer, skin testis cancer, brain tumors (gliomas), brain metastases, testicle cancer, hypophysis tumor, carcinoids, Kaposi's sarcoma, laryngeal cancer, germ cell tumor, bone cancer, colorectal carcinoma, head and neck tumors (tumors of the ear, nose and throat area), colon carcinoma, craniopharyngiomas, oral cancer (cancer in the mouth area and on lips), cancer of the central nervous system, liver cancer, liver metastases, leukemia, eyelid tumor, lung cancer, lymphomas, stomach cancer, malignant melanoma, malignant neoplasia, malignant tumors gastrointestinal tract, breast carcinoma, rectal cancer, medulloblastomas, melanoma, meningiomas, Hodgkin's/Non-Hodgkin's lymphoma, mycosis fungoides, nasal cancer, neurinoma, neuroblastoma, kidney cancer, renal cell carcinomas, oligodendroglioma, esophageal carcinoma, osteolytic carcinomas and osteoplastic carcinomas, osteosarcomas, ovarian carcinoma, pancreatic carcinoma, penile cancer, plasmacytoma, prostate cancer, pharyngeal cancer, rectal carcinoma, retinoblastoma, vaginal cancer, thyroid carcinoma, esophageal cancer, T-cell lymphoma, thymoma, tube carcinoma, eye tumors, urethral cancer, urologic tumors, urothelial carcinoma, vulva cancer, wart appearance, soft tissue tumors, soft tissue sarcoma, Nephroblastoma, cervical carcinoma, tongue cancer, invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, lobular carcinoma in situ, small-cell lung carcinoma, non-small-cell lung carcinoma, bronchial adenoma, pleuropulmonary blastoma, mesothelioma, brain stem glioma, hypothalamic glioma, cerebellar astrocytoma, cerebral astrocytoma, neuroectodermal tumor, pineal tumors, sarcoma of the uterus, salivary gland cancers, anal gland adenocarcinomas, mast cell tumors, pelvis tumor, ureter tumor, hereditary papillary renal cancers, sporadic papillary renal cancers, intraocular melanoma, hepatocellular carcinoma, cholangiocarcinoma, mixed hepatocellular cholangiocarcinoma, squamous cell carcinoma, malignant melanoma, Merkel cell skin cancer, non-melanoma skin cancer, hypopharyngeal cancer, nasopharyngeal cancer, oropharyngeal cancer, oral cavity cancer, squamous cell cancer, oral melanoma, AIDS-related lymphoma, cutaneous T-cell lymphoma, lymphoma of the central nervous system, malignant fibrous histiocytoma, lymph sarcoma, rhabdomyosarcoma, malignant histiocytosis, fibroblastic sarcoma, hemangiosarcoma, hemangiopericytoma, leiomyosarcoma (LMS), canine mammary carcinoma, and feline mammary carcinoma.

[0164] In one embodiment, the infectious disease including opportunistic diseases is selected from the group comprising or consisting of AIDS, Adenovirus Infection, Alveolar Hydatid Disease (AHD), Amoebiasis, Angiostrongyliasis, Anisakiasis, Anthrax, Babesiosis, Balantidiasis, Baylisascaris Infection, Bilharzia (Schistosomiasis), Blastocystis hominis Infection, Lyme Borreliosis, Botulism, Brainerd Diarrhea, Brucellosis, Bovine Spongiform Encephalopathy (BSE), Candidiasis, Capillariasis, Chronic Fatigue Syndrome (CFS), Chagas Disease, Chickenpox, Chlamydia pneumoniae Infection, Cholera, Chronic Fatigue Syndrome, Creutzfeldt-Jakob Disease (CJD), Clonorchiasis, Cutaneous Larva migrans (CLM), Coccidioidomycosis, Conjunctivitis, Coxsackievirus A16 (Cox A16), Cryptococcal disease, Cryptosporidiosis, West Nile fever, Cyclosporiasis, Neurocysticercosis, Cytomegalovirus Infection, Dengue Fever, Dipylidium caninum Infection, Ebola Hemorrhagic Fever (EHF), Alveolar Echinococcosis (AE), Encephalitis, Entamoeba coli Infection, Entamoeba dispar Infection, Entamoeba hartmanni Infection, Entamoeba polecki Infection, Pinworm Infection, Enterovirus Infection (Polio/Non-Polio), Epstein Barr Virus Infection, Escherichia coli Infection, Foodborne Infection, Aphthae epizooticae, Fungal Dermatitis, Fungal Infections, Gastroenteritis, Group A streptococcal Disease, Group B streptococcal Disease, Hansen's Disease (Leprosy), Hantavirus Pulmonary Syndrome, Head Lice Infestation (Pediculosis), Helicobacter pylori Infection, Hematologic Disease, Hendra Virus Infection, Hepatitis (HCV, HBV), Herpes Zoster (Shingles), HIV Infection, Human Ehrlichiosis, Human Parainfluenza Virus Infection, Influenza, Isosporiasis, Lassa Fever, Leishmaniasis, Visceral leishmaniasis (VL), Malaria, Marburg Hemorrhagic Fever, Measles, Meningitis, Mycobacterium avium Complex (MAC) Infection, Naegleria Infection, Nosocomial Infections, Nonpathogenic Intestinal Amebae Infection, Onchocerciasis, Opisthorchiasis, Papilloma virus Infection, Parvovirus Infection, Plague, Pneumocystis Pneumonia (PCP), Polyomavirus Infection, Q Fever, Rabies, Respiratory Syncytial Virus (RSV) Infection, Rheumatic Fever, Rift Valley Fever, Rotavirus Infection, Roundworms Infection, Salmonellosis, Scabies, Shigellosis, Shingles, Sleeping Sickness, Smallpox, Streptococcal Infection, Tapeworm Infection, Tetanus, Toxic Shock Syndrome, Tuberculosis, duodenum, Vibrio parahaemolyticus Infection, Vibrio septicemia, Viral Hemorrhagic Fever, Warts, Waterborne infectious Diseases, Varicella-Zoster Virus infection, Pertussis and Yellow Fever.

[0165] In one embodiment, the immunological disease and/or autoimmune disease is selected from the group comprising or consisting of: asthma, diabetes, rheumatic diseases, AIDS, rejection of transplanted organs and tissues, rhinitis, chronic obstructive pulmonary diseases, osteoporosis, ulcerative colitis, sinusitis, lupus erythematosus, recurrent infections, atopic dermatitis/eczema and occupational allergies, food allergies, drug allergies, severe anaphylactic reactions, anaphylaxis, manifestations of allergic diseases, primary immunodeficiencies, antibody deficiency states, cell mediated immunodeficiencies, severe combined immunodeficiency, DiGeorge syndrome, Hyper IgE syndrome (HIES), Wiskott-Aldrich syndrome (WAS), ataxia-telangiectasia, immune mediated cancers, white cell defects, autoimmune diseases, systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), multiple sclerosis (MS), immune-mediated or Type 1 Diabetes Mellitus, immune mediated glomerulonephritis, scleroderma, pernicious anemia, alopecia, pemphigus, pemphigus vulgaris, myasthenia gravis, inflammatory bowel diseases, Crohn's disease, psoriasis, autoimmune thyroid diseases, Hashimoto's disease, dermatomyositis, Goodpasture syndrome (GPS), myasthenia gravis (MG), Sympathetic ophthalmia, Phakogene Uveitis, chronical aggressive hepatitis, primary biliary cirrhosis, autoimmune hemolytic anemia, and Werlhof's disease.

[0166] In one embodiment, the inflammatory disease is caused, induced, initiated and/or enhanced by bacteria, viruses, prions, parasites, fungi, and/or caused by irritative, traumatic, metabolic, allergic, autoimmune, or idiopathic agents.

[0167] In one embodiment, the inflammatory disease is selected from the group comprising or consisting of inflammatory diseases of the central nervous system (CNS), inflammatory rheumatic diseases, inflammatory diseases of blood vessels, inflammatory diseases of the middle ear, inflammatory bowel diseases, inflammatory diseases of the skin, inflammatory disease uveitis, and inflammatory diseases of the larynx.

[0168] In one embodiment, the inflammatory disease is selected from inflammatory diseases of the central nervous system (CNS), inflammatory rheumatic diseases, inflammatory diseases of blood vessels, inflammatory diseases of the middle ear, inflammatory bowel diseases, inflammatory diseases of the skin, inflammatory disease uveitis, inflammatory diseases of the larynx, wherein preferably said inflammatory diseases are selected from the group comprising abscessation, acanthamoeba infection, acne vulgaris, actinomycosis, acute inflammatory dermatoses, acute laryngeal infections of adults, acute multifocal placoid pigment epitheliopathy, acute (thermal) injury, acute retinal necrosis, acute suppurative otitis media, algal disorders, allergic contact dermatitis, amyloidosis angioedema, ankylosing spondylitis, aspergillosis, atopic dermatitis, pseudorabies, autoantibodies in vasculitis, bacterial disorders, bacterial laryngitis, bacterial meningitis, Behcet's disease (BD), birdshot choroidopathy, Gilchrist's disease, Borna disease, brucellosis, bullous myringitis, bursitis, candidiasis, canine distemper encephalomyelitis, canine distemper encephalomyelitis in immature animals, canine hemorrhagic fever, canine herpes virus encephalomyelitis, cholesteatoma, chronic granulomatous diseases (CGD), chronic inflammatory dermatoses, chronic relapsing encephalomyelitis, chronic suppurative otitis media, Ocular Cicatricial pemphigoid (OCP), common upper respiratory infection, granuloma, Crohn's disease, cryptococcal disease, dermatomyositis, diphtheria, discoid lupus erythematosus (DLE), drug-induced vasculitis, drug or hypersensitivity reaction, encephalitozoonosis, eosinophilic meningoencephalitis, Erythema multiforme (EM), feline leukemia virus, feline immunodeficiency virus, feline infectious peritonitis, feline Polioencephalitis, feline spongiform encephalopathy, fibromyalgia, Fuchs Heterochromic Uveitis, gastroesophageal (laryngopharyngeal) reflux disease, giant cell arteritis, glanders, glaucomatocyclitic crisis, gonorrhea granular myringitis, Granulomatous meningoencephalitis (GME), herpes simplex, histoplasmosis, idiopathic diseases, idiopathic inflammatory disorders, immune and idiopathic disorders, infections of the immunocompromised host, infectious canine hepatitis, inhalation laryngitis, interstitial nephritis, irritant contact dermatitis, juvenile rheumatoid arthritis, Kawasaki's disease, La Crosse virus encephalitis, laryngeal abscess, laryngotracheobronchitis, leishmaniasis, lens-induced uveitis, leprosy, leptospirosis, leukemia, lichen planus, lupus, lymphoma, meningitis, meningoencephalitis in greyhounds, miscellaneous meningitis/meningoencephalitis, microscopic polyangiitis, multifocal choroiditis, multifocal distemper encephalomyelitis in mature animals, multiple sclerosis, Muscle Tension Dysphonia (MTD), mycotic (fungal) diseases, mycotic diseases of the CNS, necrotizing encephalitis, neosporosis, old dog encephalitis, onchocerciasis, parasitic encephalomyelitis, parasitic infections, Pars planitis, parvovirus encephalitis, pediatric laryngitis, pollution and inhalant allergy, polymyositis, post-vaccinal canine distemper encephalitis, prion protein induced diseases, protothecosis, protozoal encephalitis-encephalomyelitis, psoriasis, psoriatic arthritis, pug dog encephalitis, radiation injury, radiation laryngitis, radionecrosis, relapsing polychondritis, Reiter's syndrome, retinitis pigmentosa, retinoblastoma, rheumatoid arthritis, Rickettsial disorders, rocky mountain spotted fever, salmon poisoning disease (SPD), Sarcocystosis, sarcoidosis, schistosomiasis, scleroderma, Rhinoscleroma, serpiginous choroiditis, shaker dog disease. Sjogren's syndrome, spasmodic croup, spirochetal (syphilis) diseases, spongiotic dermatitis, sporotrichosis, steroid responsive meningitis-arteritis, Stevens-Johnson syndrome (SJS, EM major), epiglottitis, sympathetic ophthalmia, Syngamosis, syphilis, systemic vasculitis in sarcoidosis, Takayasu's arteritis, tendinitis (tendonitis), Thromboangiitis obliterans (Buerger Disease), tick-borne encephalitis in dogs, toxic epidermal necrolysis (TEN), toxocariasis, toxoplasmosis, trauma, traumatic laryngitis, trichinosis, trypanosomiasis, tuberculosis, tularemia, ulcerative colitis, urticaria (hives), vasculitis, vasculitis and malignancy, vasculitis and rheumatoid arthritis, vasculitis in the idiopathic inflammatory myopathies, vasculitis of the central nervous system, vasculitis secondary to bacterial, fungal, and parasitic infection, viral disorders, viral laryngitis, vitiligo, vocal abuse, vocal-cord hemorrhage, Vogt-Koyanagi-Harada syndrome (VKH), Wegener's granulomatosis, and Whipple's disease.

[0169] The present invention also relates to a method of treatment and/or prevention of a disease which is associated with inhibition of apoptosis, abnormal transcriptional activity and/or cell cycle arrest by aberrant activity and/or overexpression of one or several cyclin-dependent kinases (CDKs), in particular cyclin-dependent kinase 7 (CDK7), wherein the disease is selected from proliferative diseases, infectious diseases, including opportunistic diseases, immunological diseases, autoimmune diseases, and inflammatory diseases, wherein said method of treatment and/or prevention comprises administering a compound according to the present invention as defined herein, to a patient in need thereof.

[0170] In one embodiment, the patient in need thereof is a mammal. In one embodiment, the patient in need thereof is a human being. In another embodiment, the patient in need thereof is a non-human animal.

[0171] In one embodiment, the disease which is prevented or treated in said method is as defined herein.

[0172] The present invention also relates to the use of a compound according to the present invention as defined herein in the manufacture of a medicament for the prevention and/or treatment of a disease which is associated with inhibition of apoptosis, abnormal transcriptional activity and/or cell cycle arrest by aberrant activity and/or overexpression of one or several cyclin-dependent kinases (CDKs), in particular cyclin-dependent kinase 7 (CDK7), wherein the disease is selected from proliferative diseases, infectious diseases, including opportunistic diseases, immunological diseases, autoimmune diseases, and inflammatory diseases, as defined herein.

[0173] Further advantageous features, aspects and details of the invention are evident from the dependent claims, the description, the examples and the drawings.

[0174] The compounds of the present invention are highly efficient inhibitors of CDK7 threonine/serine kinase and/or its complex, CDK7/MAT1/CycH. The inventive compounds are suitable for the use as a pharmaceutically active agent. The inventive compounds are suitable for the treatment of disorders associated with, accompanied by, caused by and/or induced by CDK7 and its complex, in particular a hyperfunction or dysfunction thereof. The inventive compounds are thus suitable for the treatment of CDK7-associated diseases or disorders and CDK7 complex induced disorders.

[0175] The inventive compounds are also useful in the manufacture of a medicament or of a pharmaceutical composition for the treatment of disorders associated with, accompanied by, caused by and/or induced by CDK7 and its complex, in particular a hyperfunction or dysfunction thereof. The inventive compounds are further used in the manufacture of a medicament or of a pharmaceutical composition for the treatment and/or prevention of CDK7 and its complex induced disorders.

[0176] The present inventors have found that in particular in those embodiments of the present invention wherein the compounds according to the present invention contain a W-group, as defined above, they are able to bind covalently to —SH-groups of cysteine residues within cyclin-dependent kinase(s), especially CDK7, thus forming a covalent bond and an adduct between the compound and the kinase and thus inhibiting the kinase(s). This concerns in particular those embodiments wherein at least one of Z, R⁶, R⁷, R¹¹, R¹², R¹³, R¹⁵, R¹⁶ and R¹⁹ is W, as defined above or herein, or is a structure containing W, as defined above or herein.

[0177] Furthermore it concerns those embodiments wherein exactly one of Z, R⁶, R⁷, R¹¹, R¹², R¹³, R¹⁵, R¹⁶ and R¹⁹ is W, as defined above or herein, or is a structure containing W, as defined above or herein. This is because all W-structures as defined above or herein contain a double or triple bond allowing a reaction with a sulfhydryl group within the kinase and allowing the formation of an adduct between the compound and the kinase. Through the covalent binding of a compound in accordance with the present invention, the kinase is inhibited. The term “exactly one”, as used in this context, means that it is only one (and no more) of the recited groups/residues which is W or a structure containing W, as defined above or herein.

[0178] The term “optionally substituted” as used herein is meant to indicate that a hydrogen atom where present and attached to a member atom within a group, or several such hydrogen atoms, may be replaced by a suitable group, such as halogen including fluorine, C₁-C₃ alkyl, C₁-C₃ haloalkyl, methylhydroxyl, COOMe, C(O)H, COOH, OMe, or OCF₃;

[0179] The term “alkyl” refers to a monovalent straight, branched or cyclic chain, saturated aliphatic hydrocarbon radical having a number of carbon atoms in the specified range. Thus, for example, “C₁-C₆ alkyl” refers to any of the hexyl alkyl and pentyl alkyl isomers as well as n-, iso-, sec-, and t-butyl, n- and isopropyl, cyclic propyl, ethyl and methyl.

[0180] The term “alkenyl” refers to a monovalent straight or branched chain aliphatic hydrocarbon radical containing one carbon-carbon double bond and having a number of carbon atoms in the specified range. Thus, for example, “C₂-C₆ alkenyl” refers to all of the hexenyl and pentenyl isomers as well as 1-butenyl, 2-butenyl, 3-butenyl, isobutenyl, 1-propenyl, 2-propenyl, and ethenyl (or vinyl).

[0181] The term “cycloalkyl”, alone or in combination with any other term, refers to a group, such as optionally substituted or non-substituted cyclic hydrocarbon, having from three to eight carbon atoms, unless otherwise defined. Thus, for example, “C₃-C₈ cycloalkyl” refers to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.

[0182] The term “haloalkyl” refers to an alkyl group, as defined herein that is substituted with at least one halogen. Examples of straight or branched chained “haloalkyl” groups useful in the present invention include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, and t-butyl substituted independently with one or more halogens. The term “haloalkyl” should be interpreted to include such substituents such as —CHF₂, —CF₃, CH₂—CH₂—F, —CH₂—CF₃, and the like.

[0183] The term “heteroalkyl” refers to an alkyl group where one or more carbon atoms have been replaced with a heteroatom, such as, O, N, or S. For example, if the carbon atom of alkyl group which is attached to the parent molecule is replaced with a heteroatom (e.g., O, N, or S) the resulting heteroalkyl groups are, respectively, an alkoxy group (e.g., —OCH₃, etc.), an amine (e.g., —NHCH₃, —N(CH₃)₂, etc.), or thioalkyl group (e.g., —SCH₃, etc.). If a non-terminal carbon atom of the alkyl group which is not attached to the parent molecule is replaced with a heteroatom (e.g., O, N, or S) and the resulting heteroalkyl groups are, respectively, an alkyl ether (e.g., —CH₂CH₂—O—CH₃, etc.), alkyl amine (e.g., —CH₂NHCH₃, —CH₂N(CH₃)₂, etc.), or thioalkyl ether (e.g., —CH₂—S—CH₃).

[0184] The term “halogen” refers to fluorine, chlorine, bromine, or iodine.

[0185] The term “phenyl” as used herein is meant to indicate that optionally substituted or non-substituted phenyl group.

[0186] The term “benzyl” as used herein is meant to indicate that optionally substituted or non-substituted benzyl group.

[0187] The term “heteroaryl” refers to (i) optionally substituted 5- and 6-membered heteroaromatic rings and (ii) optionally substituted 9- and 10-membered bicyclic, fused ring systems in which at least one ring is aromatic, wherein the heteroaromatic ring or the bicyclic, fused ring system contains from 1 to 4 heteroatoms independently selected from N, O, and S, where each N is optionally in the form of an oxide and each S in a ring which is not aromatic is optionally S(O) or S(O)₂. Suitable 5- and 6-membered heteroaromatic rings include, for example, pyridyl, pyrrolyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, thienyl, furanyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, and thiadiazolyl. Suitable 9- and 10-membered heterobicyclic, fused ring systems include, for example, benzofuranyl, indolyl, indazolyl, naphthyridinyl, isobenzofuranyl, benzopiperidinyl, benzisoxazolyl, benzoxazolyl, chromenyl, quinolinyl, isoquinolinyl, cinnolinyl, quinazolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, isoindolyl, benzodioxolyl, benzofuranyl, imidazo[1,2-a]pyridinyl, benzotriazolyl, dihydroindolyl, dihydroisoindolyl, indazolyl, indolinyl, isoindolinyl, quinoxalinyl, quinazolinyl, 2,3-dihydrobenzofuranyl, and 2,3-dihydrobenzo-1,4-dioxinyl.

[0188] The term “heterocyclyl” refers to (i) optionally substituted 4- to 8-membered, saturated and unsaturated but non-aromatic monocyclic rings containing at least one carbon atom and from 1 to 4 heteroatoms, (ii) optionally substituted bicyclic ring systems containing from 1 to 6 heteroatoms, and (iii) optionally substituted tricyclic ring systems, wherein each ring in (ii) or (iii) is independent of fused to, or bridged with the other ring or rings and each ring is saturated or unsaturated but nonaromatic, and wherein each heteroatom in (i), (ii), and (iii) is independently selected from N, O, and S, wherein each N is optionally in the form of an oxide and each S is optionally oxidized to S(O) or S(O)₂. Suitable 4- to 8-membered saturated heterocyclyls include, for example, azetidinyl, piperidinyl, morpholinyl, thiomorpholinyl, thiazolidinyl, isothiazolidinyl, oxazolidinyl, isoxazolidinyl, pyrrolidinyl, imidazolidinyl, piperazinyl, tetrahydrofuranyl, tetrahydrothienyl, pyrazol idinyl, hexahydropyrimidinyl, thiazinanyl, thiazepanyl, azepanyl, diazepanyl, tetrahydropyranyl, tetrahydrothiopyranyl, dioxanyl, and azacyclooctyl. Suitable unsaturated heterocyclic rings include those corresponding to the saturated heterocyclic rings listed in the above sentence in which a single bond is replaced with a double bond. It is understood that the specific rings and ring systems suitable for use in the present invention are not limited to those listed in this and the preceding paragraphs. These rings and ring systems are merely representative.

Pharmaceutically Acceptable Salts

[0189] Examples of pharmaceutically acceptable addition salts include, without limitation, the non-toxic inorganic and organic acid addition salts such as the acetate derived from acetic acid, the aconate derived from aconitic acid, the ascorbate derived from ascorbic acid, the benzenesulfonate derived from benzensulfonic acid, the benzoate derived from benzoic acid, the cinnamate derived from cinnamic acid, the citrate derived from citric acid, the embonate derived from embonic acid, the enantate derived from enanthic acid, the formate derived from formic acid, the fumarate derived from fumaric acid, the glutamate derived from glutamic acid, the glycolate derived from glycolic acid, the hydrochloride derived from hydrochloric acid, the hydrobromide derived from hydrobromic acid, the lactate derived from lactic acid, the maleate derived from maleic acid, the malonate derived from malonic acid, the mandelate derived from mandelic acid, the methanesulfonate derived from methane sulphonic acid, the naphthalene-2-sulphonate derived from naphtalene-2-sulphonic acid, the nitrate derived from nitric acid, the perchlorate derived from perchloric acid, the phosphate derived from phosphoric acid, the phthalate derived from phthalic acid, the salicylate derived from salicylic acid, the sorbate derived from sorbic acid, the stearate derived from stearic acid, the succinate derived from succinic acid, the sulphate derived from sulphuric acid, the tartrate derived from tartaric acid, the toluene-p-sulphonate derived from p-toluene sulphonic acid, and the like. Such salts may be formed by procedures well known and described in the art.

[0190] Other acids such as oxalic acid, which may not be considered pharmaceutically acceptable, may be useful in the preparation of salts useful as intermediates in obtaining a chemical compound of the invention and its pharmaceutically acceptable acid addition salt.

[0191] In another embodiment, the compounds of the invention are used in their respective free base form according to the present invention.

[0192] Metal salts of a chemical compound of the invention include alkali metal salts, such as the sodium salt of a chemical compound of the invention containing a carboxy group.

[0193] The chemical compounds of the invention may be provided in unsolvated or solvated forms together with a pharmaceutically acceptable solvent(s) such as water, ethanol, and the like. Solvated forms may also include hydrated forms such as the monohydrate, the dihydrate, the hemihydrate, the trihydrate, the tetrahydrate, and the like. In general, solvated forms are considered equivalent to unsolvated forms for the purposes of this invention.

[0194] Further aspects of the present invention are illustrated and exemplified by the following schemes, examples, tables and procedural descriptions which are given merely to illustrate, not to limit the present invention. The scope of protection for the present invention is merely limited by the appended claims.

Tables

[0195] Reference is now made to tables, wherein

[0196] Table 1 shows activity data in CDK1, CDK2, CDK5 and CDK7 enzymatic assay for selected compounds of the invention. Inhibition is indicated as IC₅₀ with the following key: A=IC₅₀ less than 100 nM; B=IC₅₀ greater than 100 nM, but less than 1,000 nM; C=IC₅₀ greater than 1,000 nM. Also table 1 shows selectivity data in CDK1/CDK7, CDK2/CDK7 and CDK5/CDK7 for selected compounds of the invention. Selectivity is indicated as CDK1/CDK7*, CDK2/CDK7** and CDK5/CDK7*** with the follow key: A=greater than 500 fold; B=less than 500 fold, but greater than 50 fold; C=less than 50 fold.

[0197] Table 2 shows activity data of cellular H460 viability assay for selected compounds of the invention. Inhibition is indicated as IC₅₀ with the following key: A=IC₅₀ less than 1 uM; B=IC₅₀ greater than 1 uM, but less than 10 uM; C=IC₅₀ greater than 10 uM.

[0198] Table 3 shows activity data of cellular MV4-11 viability assay for selected compounds of the invention. Inhibition is indicated as IC₅₀ with the following key: A=IC₅₀ less than 1 uM; B=IC₅₀ greater than 1 uM, but less than 10 uM; C=IC₅₀ greater than 10 uM.

[0199] Table 4 shows activity data of A2780 viability assay for selected compounds of the invention. Inhibition is indicated as IC₅₀ with the following key: A=IC₅₀ less than 1 uM; B=IC₅₀ greater than 1 uM, but less than 10 uM; C=IC₅₀ greater than 10 uM.

[0200] Table 5 shows activity data of OVCAR-3 viability assay for selected compounds of the invention. Inhibition is indicated as IC₅₀ with the following key: A=IC₅₀ less than 1 uM; B=IC₅₀ greater than 1 uM, but less than 10 uM; C=IC₅₀ greater than 10 uM.

[0201] Table 6 shows activity data of a panel assay showing the CDK7 selectivity profile in CDKs family for compound 11 of the invention.

[0202] Table 7 summarizes compounds 1-216 in terms of their structures and corresponding characteristics.

[0203] The invention is now further described by reference to the following examples which are intended to illustrate, not to limit the scope of the invention.

Enzymatic Binding Assay Protocol for CDK1, CDK2, CDK5 and CDK7

[0204] Inhibition activity of the respective compound on CDK kinase under Km value of ATP was tested in FRET based The LANCE® Ultra kinase assay (Perkin Elmer), which uses a ULight™-labeled peptide substrate and an appropriate Europium-labeled anti-phospho-antibody. Test compounds were made with DMSO solutions, and then 4-fold serial dilutions for 8 doses were prepared using automated liquid handler (POD™ 810, Labcyte) and 80 nL/well of diluted compound solutions were added into the 384-well plates (Greiner, Cat #784075). And then 68 nM of ULight-MBP peptide (Perkin Elmer, Cat #TRF0109-M) and 5 ul/well of ATP (Sigma, Cat #A7699) were added to the plate. After 1 min centrifugation at 1000 rpm, purified CDKs/Cyclin complex were added with the following concentrations respectively. 24 uM for CDK1/Cyclin B (Invitrogen, Cat #PR4768C), 22 uM for CDK2/Cyclin A (Invitrogen, Cat #PV6290), 10 uM for CDK5/p25 (Invitrogen, Cat #PR8543B) and 400 uM for CDK7/Cyclin H/MNAT1 (Invitrogen, Cat #PR6749B) were added to each corresponding plate for CDK1, CDK2, CDK5 and CDK7. Incubate at 23° C. for 60 min and then Eu-labeled anti-phospho-Myelin Basic Protein (PE, Cat #TRF0201-M) and EDTA (Invitrogen, Cat #15575038) mixture in Lance Detection Buffer (Perkin Elmer, Cat #CR97100) was added in each well. After additional incubation at 23° C. for 60 min, test articles were measured the fluorescence using Envision leader (Perkin Elmer, USA) [Laser as excitation light; APC 615 nm and Europium 665 as the first and the second emission filter]. Data were analyzed using XL Fit software.

Cell Culture

[0205] Human T-cell acute lymphoblastic leukemia cell line, MV4-11_(ATCC, Cat #CRL-9591), NSCLC (Non-small cell lung cancer) cell line H460 (ATCC, Cat #HTB-177), A2780 (ECACC, Cat #93112519) and OVCAR-3(ATCC, Cat #HTB-161) were obtained from ATCC. Cells were grown in RPMI-1640 media (Invitrogen, Cat #22400-089) supplemented with 10% FBS (Invitrogen, Cat #10099141) and 1% penicillin/streptomycin (Invitrogen, Cat #15070063) and cultured at 37° C., 5% CO₂ in a humidified chamber. All cell lines were routinely tested for mycoplasma.

Cell H460, MV4-11, A2780 and OVCAR-3 Viability Assay Protocol

[0206] To effect of the CDK7 inhibitor to inhibit the growth of target cancer cells, viability assay were conducted a 72 hour time period. Briefly, the candidate cell line was plated in 96 well plate at the following density of cells respectively. 1×10⁴ cells/well for MV4-11, 5×10³ for H460 and OVCAR-3, and 1×10³ for A2780. After 24 hours, the cells were treated with various concentrations of the compound (ranging from 0.0015 uM to 10 uM). DMSO solvent without compound served as a control and final DMSO concentration lest than 0.1%. After 72 hours of incubation at 37° C., 5% CO₂ incubator, cells were analyzed for the viability using the CellTiter-Glo Luminescent Cell Viability Assay (Promega, Cat #G7570). All viability assays were performed in duplicate and Luminescence was read using an Envision (Perkin Elmer, USA). Data was analyzed using XLfit software.

[0207] The IC₅₀ profile of compound 11 was determined using 28 CDKs family protein kinases through ProQinase GmbH (Freiburg, Germany). All the protocol and materials had been provided by ProQinase GmbH. Briefly, in the process, 90 μl H₂O were added to each well of a compound dilution plate. To minimize potential precipitation, the H₂O was added to the plate only a few minutes before the transfer of the compound solutions into the assay plates. The plate was shaken thoroughly, resulting in a “compound dilution plate/10% DMSO”. The compound dilution plate(s) were discarded at the end of the working day. For the assays (see below), 5 μl solution from each well of the compound dilution plate were transferred into the assay plates. The final volume of the assay was 50 μl. All compounds were tested at 10 final assay concentrations in the range from 1×10⁻⁰⁵ M to 3×10⁻¹⁰ M. The final DMSO concentration in the reaction cocktails was 1% in all cases. All protein kinases provided by ProQinase were expressed in Sf9 insect cells or in E. coli as recombinant GST-fusion proteins or His-tagged proteins, either as full-length or enzymatically active fragments. All kinases were produced from human cDNAs and purified by either GSH affinity chromatography or immobilized metal affinity chromatography. The purity of the protein kinases was examined by SDS-PAGE/Coomassie staining, the identity was checked by mass spectroscopy. Kinases from external vendors, Carna Biosciences Inc.; Invitrogen Corp.; and Millipore Corp., were expressed, purified and quality-controlled by virtue of the vendors readings. A radiometric protein kinase assay (33PanQinase® Activity Assay) was used for measuring the kinase activity of the 28 protein kinases. All kinase assays were performed in 96-well FlashPlates™ from PerkinElmer (Boston, MA, USA) in a 50 μl reaction volume. The reaction cocktails were incubated at 30° C. for 60 minutes. The reaction was stopped with 50 μl of 2% (v/v) H₃PO₄, plates were aspirated and washed two times with 200 μl 0.9% (w/v) NaCl. Incorporation of ³³Pi was determined with a microplate scintillation counter (Microbeta, Wallac). All assays were performed with a BeckmanCoulter/SAGIAN™ Core System. As part of the data evaluation the low control value from a particular plate was subtracted from the high control value as well as from all 80 “compound values” of the corresponding plate. The residual activity (in %) for each well of a particular plate was calculated by using the following formula: Res. Activity (%)=100×[(cpm of compound−low control)/(high control−low control)]. Results are represented in Table 6.

[0208] Presented compounds underwent derivation according to the methods outlined below (Scheme 1-48). Resulting derivatives were examined for enzymatic binding and cellular activity (H460, MV4-11, A2780 and OVCAR-3) and for their selectivity profile in CDKs family, using the assays described above (Examples 1 to 3) and the results are summarized in Table 1-6. The synthesized compounds 1-216 are shown in Table 7.

[0209]

[0210] The method to prepare compounds of formula I-2, II-3 and III-4 were shown in Scheme 1.

[0211] Route I: Compound G10 can be treated with group A in presence of DIPEA to give compounds I-1. Compounds I-2 can be treated with HBr/AcOH to obtain the compounds of formula I-2.

[0212] Route II: Compound G10 can be treated with group B in presence of DIPEA to give compounds II-1. Compound II-1 can be treated with group C which is defined claim 1 in presence of DIPEA and acyl chloride to give compounds II-2. Compounds II-2 can be treated with HBr/AcOH to obtain the compounds of formula II-3.

[0213] Route III: Compound G10 can be treated with group D in presence of DIPEA to give compounds III-1. Compound III-1 can be treated with TFA to give compounds III-2. Compound III-2 can be treated with group C which was defined claim 1 in presence of DIPEA and acyl chloride to give compounds III-3. Compounds III-3 can be treated with HBr/AcOH to obtain the compounds of formula III-4.

General Schemes of Group A

[0214]
Procedure for Synthesis of A3

[0215] To a solution of compound A2 (2.64 g), DIPEA (3.07 g, 23.7 mmol) in DCM (40.0 mL) was added 3-nitrobenzoyl chloride A1 (2.20 g, crude) at 0° C. The reaction mixture was stirred at 10° C. for 16 hours under N₂ atmosphere. TLC showed a new spot was formed. The reaction solution was washed with water (10 mL), dried over anhydrous Na₄SO₄, filtered, concentrated under reduced pressure. The residue was purified by Combi flash to give compound A3 (1.96 g) as an off-white powder.

Procedure for Synthesis of A4

[0216] To a solution of compound A3 (1.76 g) in MeOH (40.0 mL) was added Zn powder (3.10 g, 47.40 mmol) and NH₄Cl (2.54 g, 47.4 mmol). The reaction mixture was stirred at 10° C. for 1 hour. TLC showed the reaction was completed. The reaction mixture was poured into saturated aqueous NaHCO₃ solution (20 mL) and extracted with EtOAc (10 mL×2). The combined extract was washed with brine (10 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a crude product. The crude product was purified by Combi flash to give compound A4 (875 mg) as a brown gum.

Procedure for Synthesis of A6

[0217] To a solution of compound A4 (775 mg, 2.27 mmol) and DIPEA (601 mg, 4.65 mmol) in anhydrous THF (10 mL) was added a solution of compound A5 (500 mg, 2.72 mmol) in anhydrous THF (1.0 mL) dropwise at 15° C. After stirred at 15° C. for 10 minutes, dimethylamine (2 M in THF, 7.57 mL) was added. The reaction solution was stirred at 15° C. for 20 minutes. TLC showed the reaction was complete. The reaction mixture was poured into water (10 mL) and then extracted with EtOAc (10 mL×2). The organic layer was washed with water (10 mL) and brine (10 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give the crude product as a brown gum. The crude product was purified by Combi flash to give compound A6 (337 mg) as a light brown gum.

Procedure for Synthesis of A7

[0218] To a solution of compound A6 (168 mg) in DCM (2 mL) was added TFA (500 uL). The reaction solution was stirred at 10° C. for 2 hours. TLC showed the reaction was completed. The mixture was concentrated under reduced pressure. The residue was partitioned between DCM (10 mL) and saturated aqueous NaHCO₃ solution (10 mL). The organic and aqueous layer was concentrated under reduced pressure to give 130 mg of crude compound A7. The crude product was used directly in the next step without further purification.

[0219]
Procedure for Synthesis of A10

[0220] To a solution of compound A8 (2.80 g, 12.5 mmol) in anhydrous DCM (100 mL) was added compound A9 (3.65 g, 18.8 mmol), Cu(OAc)₂ (3.42 g, 18.8 mmol) and TEA (3.81 g, 37.6 mmol, 5.22 mL). The reaction mixture was stirred at 15° C. for 1 day. TLC showed compound A13 was consumed. The reaction mixture was filtered. The filtrate was washed with water (20 mL) and concentrated under reduced pressure to give a light brown gum. The crude gum was purified by Combi flash to give compound A10 (629 mg) as a white powder.

Procedure for Synthesis of A11

[0221] To a solution of compound A10 (625 mg, 1.68 mmol) in MeOH (6 mL) was added NaOH (1 M, 3.36 mL). The reaction mixture was stirred at 15° C. for 17 hour. TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in water (5 mL) and neutralized by aqueous HCl solution (1M, 3.40 mL), then extracted with DCM (10 mL×2). The organic layer was washed with water (10 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give compound A11 (483 mg) as a white powder.

Procedure for Synthesis of A12

[0222] To a solution of compound A11 (383 mg, 1.12 mmol), benzyl alcohol (969 mg, 8.96 mmol, 931.67 uL), TEA (453 mg, 4.48 mmol, 621 uL) in dioxane (10 mL) was added DPPA (339 mg, 1.23 mmol, 267 uL). The reaction solution was heated to reflux for 2 hours. TLC showed the reaction was completed. The reaction mixture was partitioned between water (30 mL) and DCM (30 mL). The organic layer was washed with water (10 mL×2), brine (10 mL), dried over anhydrous Na₂SO₄, and concentrated under reduced pressure to give a residue. The crude product was purified by Combi flash to give compound A12 (1.20 g, crude) as a colorless oil. The crude product was used directly in the next step without further purification.

Procedure for Synthesis of A13

[0223] To a solution of compound A12 (1.10 g, crude) in MeOH (50 mL) was added Pd/C (100 mg, 50% wet, 10% Pd). The reaction mixture was degassed under vacuum and purged with H₂ for 3 times, then stirred at 15° C. for 16 hours under H₂ atmosphere (15 psi). TLC showed the reaction was completed. The reaction mixture was filtered through a pad of Celite. The filtrate was concentrated under reduced pressure. The residue was purified by Combi flash to give compound A13 (210 mg) as a colorless oil.

Procedure for Synthesis of A15

[0224] To a solution of compound A13 (140 mg, 0.445 mmol), TEA (64 mg, 0.63 mmol) in DCM (2 mL) was added acryl chloride A14 (61.0 mg, 0.674 mmol) dropwise at 20° C. The reaction solution was stirred at 20° C. for 2 hours under N₂ atmosphere. TLC showed the reaction was completed. The reaction was quenched with water (5 mL) and extracted with DCM (10 mL×2). The combined extract was washed with water (5 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give the crude product as a brown gum. The crude product was purified by Combi flash to give compound A15 (131 mg) as a brown gum.

Procedure for Synthesis of A16

[0225] The compound A15 (130 mg) was followed the same procedure of A7 to obtain 90 mg of compound A16 as a brown gum.

Procedure for Synthesis of A17

[0226] To a solution of compound A13 (210 mg, 0.668 mmol) and DIPEA (177 mg, 1.37 mmol) in anhydrous THF (5 mL) was added a solution of compound A5 (147 mg, 0.801 mmol) in anhydrous THF (1.0 mL) dropwise at 15° C. After stirred at 15° C. for 30 minutes, LCMS showed the desired product. The reaction mixture was poured into water (10 mL) and then extracted with DCM (10 mL×2). The organic layer was washed with water (10 mL) and brine (10 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give the crude product as a brown gum. The crude product was purified by Combi flash to give compound A17 (183 mg) as a light brown gum.

Procedure for Synthesis of A18

[0227] The compound A17 (180 mg) was followed the same procedure of A7 to obtain 133 mg of compound A18 as a brown gum.

[0228]
Procedure for Synthesis of 21

[0229] To a solution of compound A20 (300 mg, 1.68 mmol) and compound A19 (506 mg, 2.02 mmol) in dioxane (5 mL) and H₂O (1 mL) was added Cs₂CO₃ (547 mg, 1.68 mmol), Pd(dppf)Cl₂ (123 mg, 0.168 mmol) under N₂. The resulting mixture was heated at 100° C. and stirred for 1.5 hours to give black suspension. LCMS and TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by combi flash to give compound A21 (240 mg) as a yellow solid.

Procedure for Synthesis of A22

[0230] The compound A21 (408 mg) was followed the same procedure of A6 to obtain 184 mg of compound A22 as a yellow oil.

Procedure for Synthesis of A23

[0231] The compound A22 (184 mg) was followed the same procedure of A7 to obtain 160 mg of compound A23 as a yellow oil.

General Schemes of Group B

[0232]
Procedure for Synthesis of B3

[0233] To a solution of compound B1 (2.48 g, 8.66 mmol), compound B2 (1.00 g, 7.87 mmol), pyridine-2-carboxylic acid (194 mg, 1.57 mmol) and K₃PO₄ (3.34 g, 15.7 mmol) in DMSO (15 mL) was added CuI (150 mg, 0.787 mmol), the mixture was purged with N₂ for three times and stirred at 90° C. for 17 hours to give a dark solution. LCMS showed the reaction was completed. TLC showed the reaction was completed. The reaction mixture was poured into water (100 mL), extracted with EtOAc (100 mL×2), the combined extracts was washed with brine (30 mL×2), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to give compound B3 (860 mg) as light yellow oil.

Procedure for Synthesis of B4

[0234] To a solution of compound B3 (860 mg, 2.59 mmol) in DCM (7 mL) was added TFA (3 mL), the reaction mixture was stirred at 25° C. under N₂ for 1 hour to give a brown solution. TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give compound B4 (800 mg) as brown oil.

[0235]
Procedure for Synthesis of B6

[0236] To a suspension of compound B5 (4.00 g, 25.2 mmol) and Cs₂CO₃ (16.4 g, 50.5 mmol) in DMF (50 mL) was added 3-cyanophenol (3.16 g, 26.5 mmol), the mixture was stirred at 60° C. for 17 hours to give a brown suspension. Crude LCMS (RT: 1.384 min) showed the reaction was completed. The mixture was poured into water (400 mL), a lot of white solid appeared, filtered, the filter cake was washed with water (30 mL×3) to give the crude product. The crude product was purified by Combi flash to give 1.00 g of compound B6 as a yellow powder.

Procedure for Synthesis of B7

[0237] To a solution of compound B6 (850 mg, 3.52 mmol) and Pd/C (170 mg, 10% Pd) in MeOH (10 mL) was added NH₃·H₂O (1.83 g, 5.21 mmol), the mixture was purged with N₂ for three times and stirred at 20° C. under H₂ balloon (15 psi) for 1 hour to give a brown suspension. The crude LCMS showed the reaction was completed. The mixture was filtered, the filtrate was concentrated under reduced pressure to give 700 mg of compound B7 as a yellow gum.

[0238]
Procedure for Synthesis of B10

[0239] To a solution of NaH (1.73 g, 43.4 mmol) in DMF (100 mL) was added 7-nitro-2H-indazole B8 (5.19 g, 31.8 mmol) in several portion at 20° C., the resulting mixture was stirred for 1 hour at 20° C., then 2-fluorobenzonitrile B9 (3.50 g, 28.9 mmol) was added to the mixture, the reaction mixture was stirred for another 12 hours at 130° C. to give black suspension. TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (500 mL) and extracted with EtOAc (500 mL×2). The combined organic layers were washed with brine (100 mL×2), dried over Na₇SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by triturated to obtain compound B10 (1.80 g) as a black solid.

Procedure for Synthesis of B11

[0240] To a solution of compound B10 (200 mg, 0.8 mmol) in MeOH (20 mL) and NH₃·H₂O (1.00 mL, 25%) was added Raney-Ni (64.8 mg, 0.8 mmol) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H₂ (40 psi) at 20° C. for 2 hours to give black suspension. TLC and LCMS showed the reaction was completed. The reaction mixture was filtered by celite pad and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to obtain compound B11 (50 mg) as a yellow oil.

[0241]
Procedure for Synthesis of B13

[0242] To a solution of compound B12 (1.50 g, 9.25 mmol) in MeOH (50 mL) was added Zn (6.05 g, 92.5 mmol) and NH₄Cl (4.95 g, 92.5 mmol). The resulting mixture was stirred at 20° C. for 12 hours to give black suspension. TLC showed the reaction was completed, one new spot was formed. The reaction mixture was filtered and concentrated under reduced pressure to give a residue to give 1.80 g compound B13 as a black solid and used in the next step without purification.

Procedure for Synthesis of B14

[0243] To a solution of crude product compound B13 (1.80 g, 6.81 mmol) in MeOH (50 mL) was added Et₃N (689 mg, 6.81 mmol) and Boc₂O (2.23 g, 10.2 mmol). The resulting mixture was stirred at 20° C. for 12 hours to give black solution. TLC showed one new spot was formed. The reaction mixture was filtered under reduced pressure to give a residue. The residue was purified by Combi flash to obtain compound B14 (781 mg) as a white solid.

Procedure for Synthesis of B16

[0244] To a mixture of compound B14 (810 mg, 3.23 mmol), compound B15 (500 mg, 2.15 mmol) in HOAc (20 mL) was added Pd(OAc), (241 mg, 1.08 mmol), the mixture was stirred at 40-50° C. under O₂ (15 psi) atmosphere for 12 hours to give a black brown suspension. LCMS (Rt=1.436 min) showed the reaction was completed. AcOH was removed under reduced pressure, and the residue was dissolved in DCM (150 mL) and washed with saturated aqueous NaHCO₃ (100 mL×3). The organic layer was dried over Na₂SO₄, filtered, concentrated under reduced pressure to give black brown oil. The mixture was for Combi flash to give compound B16 (380 mg) as a yellow gum.

Procedure for Synthesis of B17

[0245] To a mixture of compound B16 (380 mg, 0.869 mmol) in DCM (30 mL) was added TFA (8 mL). The mixture was stirred at 15° C. for 0.5 hour to give a yellow mixture. LCMS showed the reaction was completed. The mixture was combined and concentrated under reduced pressure to give compound B17 (350 mg) as yellow oil

[0246]
Procedure for Synthesis of B19

[0247] A solution of 2-chloroquinoline B18 (2.00 g, 12.2 mmol) in H₂SO₄ (20 mL) was cooled to 0° C. HNO₃ (3.55 g, 36.7 mmol) was added dropwise. The reaction solution was stirred at 25° C. for 1 hour to give a black brown solution. TLC showed the reaction was completed. The reaction solution was poured into water (50 mL), neutralized to pH=7-8 with saturated Na₂CO₃. The resulting mixture was extracted with DCM (200 mL×2). The combined organic layer was washed with brine (200 mL), dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound B19 (1.30 g) as a yellow solid.

Procedure for Synthesis of B21

[0248] To a solution of compound B19 (560 mg, 2.68 mmol) and compound B20 (2.02 g, 8.04 mmol) in dioxane (10 mL)/H₂O (3 mL) was added Cs₂CO₃ (1.75 g, 5.36 mmol) and Pd(dppf)Cl₂ (98.1 mg, 0.134 mmol) under N₂ atmosphere. The reaction mixture was heated to 100° C. and stirred for 16 hours under N₂ atmosphere to give a black mixture. TLC showed the reaction was completed. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (200 mL×2). The combined extracts were dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound B21 (1.00 g) as brown solid.

Procedure for Synthesis of B22

[0249] To a solution of compound B21 (500 mg, 1.32 mmol) and NH₄C1 (706 mg, 13.2 mmol) in MeOH (10 mL) was added Zn (863 mg, 13.2 mmol) slowly. The reaction mixture was stirred at 25° C. for 16 hours to give a black brown mixture. TLC showed the reaction was completed. The reaction mixture was diluted with MeOH (50 mL) and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by Combi Flash to give compound B22 (500 mg) as a yellow solid.

Procedure for Synthesis of B23

[0250] To a solution of compound B22 (500 mg, 1.43 mmol) in DCM (7 mL) was added TFA (3 mL). The reaction solution was stirred at 25° C. for 1 hour to give a red solution. LCMS showed the reaction was completed. The reaction was diluted with DCM (10 mL) and concentrated under reduced pressure to give compound B23 (300 mg) as black brown oil.

[0251]
Procedure for Synthesis of B25

[0252] Isoquinolin-6-amine B24 (2.00 g, 13.87 mmol) was dissolved in pyridine (20 mL), and 4-methylbenzenesulfonyl chloride (3.17 g, 16.64 mmol) was added. The reaction mixture was stirred at 20° C. for 12 hours. LCMS showed the reaction was completed. To the reaction mixture was added water (30 mL) under good stirring, the mixture was stirred at 20° C. for 0.5 hour, pale yellow solid precipitated out. The mixture was filtered and the solid was collected and washed with water (5 mL) to give compound B25 (2.2 g) as a yellow solid.

Procedure for Synthesis of B26

[0253] Compound B25 (2.00 g, 6.70 mmol) was dissolved in CHCl₃ (30.00 mL). Under ice-cooling (0° C.), m-CPBA (1.71 g, 7.91 mmol) was added thereto, followed by stirring at 20° C. for 12 hours. TLC showed the reaction was completed. The solvent was evaporated and the resulting solid were washed with MTBE (50 mL). The filter cake was collected and dried in high vacuum to give compound B26 (1.96 g) as a light yellow solid.

Procedure for Synthesis of B27

[0254] To a mixture of compound B26 (4.20 g, 13.4 mmol) in CHCl₃ (120 mL) was added POCl₃ (45.1 g, 293.9 mmol). The reaction mixture was heated to 61° C. and stirred for 16 hours to give a black brown solution. TLC showed the reaction was completed. The reaction solution was cooled to 20° C. and concentrated under reduced pressure. The residue was poured into water (200 mL) and neutralized to pH=8-9 with saturated Na₂CO₃. 300 mL EtOAc was added and the mixture was filtered. The filtrate was collected, separated and the aqueous phase was extracted with EtOAc (200 ml×2). The combined extracts were collected, dried over anhydrous Na₂SO₄ and concentrated under reduced pressure to give compound B27 (4.00 g) as a yellow solid.

Procedure for Synthesis of B28

[0255] A solution of compound B27 (4.00 g, 12.0 mmol) in H₂SO₄ (50 mL) (90%) was stirred at 20° C. for 16 hours to give a black brown solution. LCMS showed the reaction was completed. The reaction solution was cooled to 0-10° C. with ice-water (100 mL), neutralized to pH=7-8 with Na₂CO₃ (solid) and extracted with EtOAc (300 mL×2). The combined extracts were collected, dried over anhydrous Na₂SO₄ and concentrated under reduced pressure to give compound B28 (1.80 g) as a red solid.

Procedure for Synthesis of B30

[0256] To a solution of compound B28 (1.00 g, 5.60 mmol) and compound B29 (4.22 g, 16.8 mmol) in dioxane (15 mL)/H₂O (5 mL) was added Cs₂CO₃ (3.65 g, 11.2 mmol) and Pd(dppf)Cl₂ (205 mg, 0.280 mmol) under N₂ atmosphere. The reaction mixture was heated to 100° C. and stirred for 4 hours under N₂ atmosphere to give a black mixture. TLC showed the reaction was completed. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (200 mL×2). The combined extracts were dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound B30 (1.00 g) as black brown oil.

Procedure for Synthesis of B31

[0257] To a solution of compound B30 (1.00 g, 2.86 mmol) in DCM (14 mL) was added TFA (6 mL) slowly. The reaction solution was stirred at 25° C. for 1 hour to give a red solution. LCMS showed the reaction was completed. The reaction solution was concentrated under reduced pressure to give compound B31 (1.00 g) as black brown oil, used for next step without further purification.

[0258]
Procedure for Synthesis of B33

[0259] To a solution of compound B19 (2.7 g, 12.9 mmol, 1 eq) and compound 32 (3.15 g, 12.9 mmol, 1.0 eq) in dioxane (50 mL) and H₂O (10 mL) were added Na₂CO₃ (2.74 g, 25.9 mmol, 2 eq) and Pd(PPh₃)₄ (748 mg, 0.65 mmol, 0.05 eq) under N₂. The resulting mixture was heated at 80° C. and stirred for 12 hrs to give yellow suspension. TLC showed the reaction was completed. The reaction mixture was filtered to give a residue as a light yellow solid. Then the residue was dissolved in DCM (200 mL) and H₂O (200 mL), and extracted with DCM (200 mL). The combined organic layers were washed with brine (100 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give compound B33 (3.25 g) as a light yellow solid.

Procedure for Synthesis of B34

[0260] To a solution of compound B33 (2.5 g, 8.64 mmol, 1 eq) in DCM (100 mL) was added Pd/C (1.5 g, 1.75 mmol) under N₂. The suspension was degassed under vacuum and purged with H, several times. The mixture was stirred under H₂ (15 psi) at 15° C. for 12 hours to give black solution. LCMS showed the reaction was completed. The reaction mixture was filtered and concentrated under reduced pressure to give compound B34 (1.96 g) as a yellow solid.

Procedure for Synthesis of B35

[0261] To a suspension of LiAlH₄ (673 mg, 17.7 mmol, 2 eq) in THF (20 mL) was added a solution of compound B34 (2.3 g, 8.87 mmol, 1 eq) in THF (10 mL) at 0° C. The reaction mixture was stirred at 15° C. for 1 hour to give red solution. LCMS showed the reaction was completed. The mixture was quenched by saturated NH₄Cl solution. The mixture was partitioned between EtOAc and H₂O. The aqueous phase was extracted with EtOAc. The combined organic was washed with brine (200 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to afford compound B35 (1.53 g, crude) as a brown solid. The crude product was used in the next step directly.

General Schemes of Group D

[0262]
Procedure for Synthesis of D2

[0263] To a solution of compound D1 (500 mg, 2.32 mmol) and 3-hydroxybenzonitrile (276 mg, 2.32 mmol) in THF (20 mL) was added PPh₃ (730 mg, 2.78 mmol) and DEAD (485 mg, 2.78 mmol). The resulting mixture was stirred at 20° C. for 12 hour to give yellow solution. LCMS and TLC showed the reaction completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (30 mL×2), dried over Na₂SO₁, filtered and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to obtain compound D2 (587 mg) as a yellow oil

Procedure for Synthesis of D3

[0264] To a solution of compound D2 (587 mg, 1.86 mmol) in MeOH (20 mL) and NH₃·H₂O (1 mL) (28%) was added Raney-Ni (159 mg, 1.86 mmol) under N₂. The suspension was degassed under vacuum and purged with H₂ several times. The mixture was stirred under H₂ (15 psi) at 20° C. for 2 hours to give black suspension. LCMS showed the reaction was completed. The reaction mixture was filtered by celite pad and concentrated under reduced pressure to give compound D3 (600 mg) as yellow oil,

[0265]
Procedure for Synthesis of D5

[0266] To tert-butyl 4-hydroxypiperidine-1-carboxylate (4.82 g, 23.95 mmol) in DMF (50 mL) was added portionwise NaH (1.44 g, 35.92 mmol) at 0° C. The reaction mixture was stirred at 20° C. for 2 hours. Then 2-fluorobenzonitrile D4 (2.90 g, 23.95 mmol) was added the above mixture and the reaction mixture was heated to 50° C. for 1 hour. TLC showed the reaction was completed. Saturated NH₄Cl (100 mL) was added dropwise into the reaction mixture carefully at 0° C. to quench the reaction. The mixture was extracted with EtOAc (100 mL×2). The combined extracts were washed with water (50 mL×3), brine (100 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give compound D5 (9.10 g, crude) as a light yellow oil.

Procedure for Synthesis of D6

[0267] To a mixture of Raney-Ni (425 mg, 4.96 mmol) and compound D5 (3.00 g, 9.92 mmol) in MeOH (90 mL) was added NH₃H₂O (6 mL) under N₂ atmosphere. The suspension was degassed under vacuum and purged with H₂ three times. The mixture was stirred under H₂ (15 psi) at 20° C. for 4 hours. LCMS showed the reaction was completed. The reaction mixture was filtered, the filtrate was concentrated to remove most MeOH. The residue was diluted with DCM (100 mL), washed with brine (80 mL×2), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give compound D6 (2.90 g) as a light yellow oil.

[0268]

[0269] The method to prepare compounds of formula IV-5 and IV-6 is shown in Scheme 14.

[0270] Route IV: Compound G24 can be treated with group E in presence of DIPEA to give compounds IV-1. Compound IV-1 can be treated with mCPBA or Oxone to give compounds IV-2. Compound IV-2 can be treated with group F in presence of DIPEA or NaH to give compounds IV-3. Compound IV-3 can be treated with Pd/C and H₂, or HCl to give compounds IV-4. Compound IV-4 can be treated with group C which was defined claim 1 to give compounds IV-5. Compounds IV-5 can be treated with acid such as HCl to obtain the compounds of formula IV-6.

General Schemes of Group E

[0271]
Procedure for Synthesis of E2

[0272] To a solution of E1 (93 g, 476 mmol) in DMF (45 mL) was added 1-tert-butoxy-N,N,N,N′-tetramethyl-methanediamine (249 g, 1.43 mol, 295 mL). The reaction mixture was stirred at 140° C. for 3 hr to give a brown mixture. TLC showed new spot. The mixture was cooled to room temperature and stirred at 0° C. for 30 min. Solid was precipitated out. After filtration, the filter cake was washed with EtOAc/PE and dried under reduced pressure to give compound E2 (69 g) as a purple powder.

Procedure for Synthesis of E3

[0273] A solution of E2 (63 g, 252 mmol), (2,4-dimethoxyphenyl)methanamine (63 g, 378 mmol, 57 mL) in toluene (150 mL) was stirred at 35° C. for 2 hours to give a yellow mixture. Then the reaction was stirred at 65° C. for 2 hours to give a yellow mixture. Then the reaction was stirred at 110° C. for 3 hours to give a yellow mixture. TLC showed new spot. The mixture was cooled to 20° C. The yellow solid was precipitated out. The mixture was filtered. The filter cake was washed with PE (50 mL) for twice and dried over high vacuum to give compound E3 (50 g) as yellow solid.

Procedure for Synthesis of E4

[0274] A solution of E3 (55 g, 162 mmol) in TFA (330 mL) was stirred at 70° C. for 16 hours to give a purple mixture. TLC showed new spot. The reaction mixture was concentrated under reduced pressure to give a residue. The residue was added PE (60 mL), and stirred at 25° C. for 2 hours to give a purple mixture. After filtration, the filter cake was washed with PE (50 mL), dried under reduced pressure to give compound E4 (80 g, crude) as purple solid.

Procedure for Synthesis of E5

[0275] A solution of E4 (80 g, 421 mmol) in POCl₃ (341 mL) was stirred at 100° C. for 2 hours to give a brown mixture. TLC showed new spot. The reaction mixture was concentrated under reduced pressure to give a residue. The residue was dissolved in DCM (1000 mL). The organic layer was washed with saturated NaHCO₃ solution (1000 mL), solid was precipitated out. After filtration, the filter cake was washed with DCM (300 mL×2). The organic layer was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a crude product. The residue was purified by column chromatography to give compound E5 (35 g) as light yellow solid.

Procedure for Synthesis of E7

[0276] To a solution of E6 (40 g, 183 mmol) in MeCN (400 mL) was added NBS (35.9 g, 202 mmol), BPO (444 mg, 1.83 mmol). The reaction mixture was stirred at 90° C. for 4 hours to give a brown mixture. LCMS showed the desired MS. The reaction mixture was diluted with water (200 mL) and extracted with EtOAc (100 mL*2). The organic layer was washed with water (100 mL*4), brine (100 mL*3), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give E7 (57 g, crude) as brown oil.

Procedure for Synthesis of E8

[0277] A mixture of E7 (57 g, 192 mmol) and NaN3 (18.8 g, 290 mmol) in DMSO (290 mL) was stirred at 25° C. for 16 hours to give a brown mixture. LCMS showed the desired MS. The reaction mixture was quenched with NaHCO₃ (500 mL) and extracted with EtOAc (200 mL*2). The organic layer was washed with water (300 mL*4), brine (300 mL*4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give E8 (42 g, crude) as brown oil.

Procedure for Synthesis of E9

[0278] To a solution of E5 (12 g, 46.3 mmol) in dioxane (60 mL) and H₂O (15 mL) was added E5 (9.66 g, 46.3 mmol), Cs₂CO₃ (30.2 g, 92.6 mmol, 2 eq) and Pd(dppf)Cl₂ (1.69 g, 2.32 mmol, 0.05 eq). The reaction mixture was stirred at 80° C. under N₂ atmosphere protect for 5 hours to give a black mixture. TLC showed new spot. The reaction mixture was diluted with water (300 mL) and extracted with EtOAc (200 mL*2). The organic layer was washed with water (100 mL*4), brine (100 mL*2), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to give E9 (8 g) as brown solid.

Procedure for Synthesis of E10

[0279] To a solution of E9 (8 g, 26.2 mmol, 1 eq) in THF (80 mL)/H₂O (40 mL) was added PPh₃ (10.3 g, 39.3 mmol, 1.5 eq). The reaction mixture was stirred at 60° C. for 16 hours to give a brown mixture. TLC showed the reaction completed. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL*2). The organic layer was washed with brine (100 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a E10 (7.32 g, crude) as brown gum.

[0280]
Procedure for Synthesis of E12

[0281] To a mixture of E11 (2 g, 8.93 mmol) in pyridine (20 mL) was added Tf₂O (3.02 g, 10.71 mmol, 1.77 mL, 1.2 eq) at 0° C., the mixture was stirred at 0° C. for 2 hours to give a brown mixture. LCMS showed the reaction was completed. The reaction mixture was quenched with water (20 mL) and extracted with EtOAc (20 mL×2). The organic layer was washed with water (20 mL×2), brine (30 mL×4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford E12 (2.2 g) as a white solid.

Procedure for Synthesis of E13

[0282] The compound E13 (2.2 g) was followed the same procedure of B33 to obtain 1.3 g of compound E13 as a yellow powder.

Procedure for Synthesis of E14

[0283] To a mixture of E13 (600 mg, 1.77 mmol) and NH₂Boc (248 mg, 2.12 mmol) in dioxane (10 mL) was added Pd(OAc)₂ (39.71 mg, 176.89 umol) and Xantphos (204 mg, 353.79 umol) and Cs₂CO₃ (1.15 g, 3.54 mmol), the mixture was stirred at 100° C. for 16 hours to give a black mixture. TLC showed the reactant was consumed. The reaction mixture was quenched with water (20 mL) and extracted with EtOAc (20 mL×2). The organic layer was washed with water (20 mL×2), brine (30 mL×4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford E14 (190 mg) as a yellow solid.

Procedure for Synthesis of E15

[0284] The compound E14 (400 mg) was followed the same procedure of B11 to obtain 385 mg of compound E15 as a yellow gum.

[0285]
Procedure for Synthesis of E16

[0286] The compound B12 (10.2 g) was followed the same procedure of B14 to obtain 15.2 g of compound

[0287] E16 as a yellow powder.

Procedure for Synthesis of E17

[0288] To a solution of compound E16 (7 g, 26.7 mmol) in THF (45 mL) was added LDA (2 M, 20 mL) at −78° C. under N₂. The reaction was stirred at −78° C. for 30 min. Tributyl(chloro)stannane (10.4 g, 32 mmol, 1.2 eq) was added into the reaction at −78° C. The reaction was stirred at −78° C. for 30 min and the reaction was stirred at 15° C. for 17 hours to give a yellow mixture. TLC showed the starting material was not consumed completely. Saturated NH₄Cl (20 mL) was added into the reaction mixture. The mixture was partitioned between EtOAc (300 mL) and H₂O (300 mL). The organic extract was washed with saturated NH₄Cl (300 mL), brine (300 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give yellow gum. The crude product was purified by combi flash to give compound E17 (9.8 g) as yellow oil.

Procedure for Synthesis of E19

[0289] To a suspension of compound E18 (1 g, 5.10 mmol) in THF (10 mL) was added BH₃·THF (1 M, 15.3 mL) under N₂ atmosphere at 0° C. The reaction was stirred at 15° C. for 30 min to give a yellow mixture. LCMS showed the starting material was not consumed completely. The reaction was stirred at 15° C. for 17 hours to give a yellow mixture. LCMS showed the starting material was consumed completely. Little mixture was purified by prep-TLC to give a sample. The reaction was quenched with MeOH (4 mL). The reaction mixture was concentrated under reduced pressure to give E19 (1.1 g, crude) as a yellow gum.

Procedure for Synthesis of E20

[0290] The compound B19 (1.1 g) was followed the same procedure of B14 to obtain 890 mg of compound E20 as a colorless oil.

Procedure for Synthesis of E21

[0291] The compound E20 (800 mg) and E17 (1.91 g) was followed the same procedure of B33 to obtain 385 mg of compound E21 as a yellow oil.

Procedure for Synthesis of E22

[0292] The compound E21 (600 mg) was followed the same procedure of A7 to obtain 450 mg of compound E22 as a yellow powder.

[0293]
Procedure for Synthesis of E24

[0294] To a solution of E23 (5.7 g, 20.56 mmol) in THF (60 mL) was added Pd/C (2 g, 10% purity) under N₂ atmosphere. The suspension was degassed and purged with H2. The mixture was stirred under H₂ (15 psi) at 25° C. for 16 hr to give a black mixture. TLC showed new spot. The reaction was diluted with THF (200 mL) and filtered over celite pad. The filtrate was concentrated under reduced pressure to give E24 (6.3 g, crude) as yellow solid.

Procedure for Synthesis of E25

[0295] To a solution of E24 (3 g, 12.13 mmol) in THF (30 mL) was added LAH (920.87 mg, 24.26 mmol). The mixture was stirred at 25° C. for 3 hr to give a yellow mixture. TLC showed new spot. The reaction mixture was quenched with water (50 mL) and extracted with EtOAc (30 mL*2). The reaction mixture was concentrated under reduced pressure to remove solvent. The combined organic layers were washed with brine (30 mL*2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to give E25 (3 g, crude) as brown oil.

[0296]
Procedure for Synthesis of E27

[0297] To a solution of E26 (8 g, 37.72 mmol) and NaHCO₃ (4.75 g, 56.58 mmol, 2.20 mL) in Water (40 mL) and THF (80 mL) was added benzyl (2, 5-dioxopyrrolidin-1-yl) carbonate (9.87 g, 39.61 mmol). The reaction was then stirred at 25° C. for 15 h to give yellow suspension. The reaction was diluted with EA (200 mL), washed with water (150 mL*2), 0.5M HCl (150 mL) and brine (150 mL). The organic layer was collected, dried over Na₂SO₄, concentrated in vacuum to give E27 (12.45 g, 35.96 mmol, 95.33% yield) as yellow oil.

Procedure for Synthesis of E28

[0298] A mixture of E27 (4 g, 11.55 mmol), E8 (3.59 g, 13.86 mmol), Na₂CO₃ (3.06 g, 28.88 mmol) and Pd(dppf)Cl₂ (507.22 mg, 693.21 umol) in dioxane (40 mL) and H₂O (10 mL) was purged with N₂, then, heated at 80° C. under N₂ atmosphere for 15 h to give a brown mixture. The mixture was poured into H₂O (50 mL) and extracted with EtOAc (50 mL*3), the organic layer was washed with brine (50 mL*10), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give residue as yellow solid. The residue was purified by silica gel chromatography to give E28 (2.15 g, 5.40 mmol, 46.70% yield) as white solid.

Procedure for Synthesis of E29

[0299] To a mixture of E28 (2.15 g, 5.40 mmol) in THF (20 mL), H₂O (5 mL) was added PPh₃ (1.70 g, 6.47 mmol), and the mixture was stirred for 2 h at 50° C. to give a colorless mixture. The mixture was poured into H₂O (60 mL) and extracted with EtOAc (60 mL*3), the organic layer was washed with brine (60 mL*10), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give E29 (2.51 g, crude) as yellow oil.

[0300]
Procedure for Synthesis of E31

[0301] To a solution of E30 (9.94 g, 84.14 mmol) in DMF (80 mL) was added 1,1-dimethoxy-N,N-dimethyl-methanamine (51.68 g, 420.70 mmol), the resulting mixture was stirred at 130° C. for 16 hours to give brown solution. The reaction mixture was concentrated under reduced pressure to give E31 (10.6 g, 61.20 mmol, 72.73% yield) was obtained as black solid.

Procedure for Synthesis of E32

[0302] To a solution of E31 (4.3 g, 24.82 mmol) in EtOH (45 mL) was added HBr (75.35 g, 372.49 mmol, 50.57 mL) dropwise slowly, the resulting mixture stirred at 90° C. for 16 h under N₂ to give yellow solution. LCMS showed the reaction was completed. The reaction mixture diluted with water 20 mL and extracted with EtOAc (20 mL×3). The aqueous layers was basified with Na₂CO₃ to pH=6 and extracted with EA/MeOH. The crude product was purified by flash column to give E32 (1.67 g, 11.43 mmol, 46.03% yield) was obtained as yellow solid.

Procedure for Synthesis of E33

[0303] To a solution of E32 (1.4 g, 9.58 mmol) in MeCN (20 mL) was added BnBr (1.97 g, 11.50 mmol, 1.37 mL), the resulting mixture was stirred at 90° C. for 2 hours to give yellow solution, then the mixture cooled to 20° C., the mixture removed under reduced pressure and the residue dissolved in EtOH (20 mL) and cooled to 0° C. NaBH₄ (7 eq) was added portion wise over 30 min and the mixture warmed to 20° C. as the ice bath melted, then the resulting mixture was stirred at 20° C. for 24 hours to give yellow solution. The reaction mixture was carefully acidified to pH=3 with 1N HCl and stirred for 30 min at r.t. The solution was concentrated under reduced pressure. The residue was neutralized with sat. NaHCO₃ aq. (100 mL) and was extracted with DCM (100 mL×3). The combined organic layers were concentrated under reduced pressure. The crude product was purified by flash column to afford E33 (1.5 g, 6.24 mmol, 65.16% yield) was obtained as yellow solid.

Procedure for Synthesis of E34

[0304] A solution of E33 (1 g, 4.16 mmol) in POCK (12.76 g, 83.23 mmol) was stirred at 100° C. for 16 hours to give yellow solution. The solvent was removed under reduced pressure and the residue quenched with saturated aqueous NaHCO₃ (70 mL). The mixture was extracted with DCM (50 mL×4). The combined organic layers were washed with brine (50 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure. The crude product was purified by flash column to give E34 (930 mg, 3.59 mmol, 86.37% yield) was obtained as white solid.

Procedure for Synthesis of E36

[0305] To a solution of E34 in dioxane (6 mL) and H₂O (1.5 mL) was added E35 (824.23 mg, 2.47 mmol), Pd(dppf)Cl₂ (56.56 mg, 77.30 umol), Na₂CO₃ (409.63 mg, 3.86 mmol). The reaction mixture was stirred at 80° C. for 5 hours to give a black mixture. The mixture was partitioned between EtOAc (20 mL) and H₂O (20 mL). The aqueous phase was extracted with EtOAc (20 mL×2). The combined organic extract was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica column to afford E36 (620 mg, 1.44 mmol, 93.37% yield) as a yellow solid

Procedure for Synthesis of E37

[0306] To a solution of E36 (620 mg, 1.44 mmol) and HCl (12 M, 240.56 uL) in EtOH (10 mL) was Pd/C (300 mg, 144.34 umol), the mixture was stirred at 25° C. under H₂ atmosphere for 3 hours to give a black mixture. The reaction mixture was filtered and concentrated under reduced pressure to give E37 (650 mg, crude) as a yellow gum.

Procedure for Synthesis of E38

[0307] To a solution of E37 (650 mg, 1.91 mmol) in THF (10 mL) and H₂O (5 mL) was added CbzOSu (620.42 mg, 2.49 mmol) and NaHCO₃ (321.75 mg, 3.83 mmol). The mixture was stirred at 25° C. for 1 hours to give a yellow mixture. The reaction mixture was quenched by addition of water (20 mL), and then extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica column to afford E38 (680 mg, 1.44 mmol, 74.98% yield) as a yellow oil.

Procedure for Synthesis of E39

[0308] To a solution of E38 (680 mg, 1.44 mmol) in DCM (7 mL) was added TFA (2.46 g, 21.54 mmol, 1.59 mL). The mixture was stirred at 15° C. for 2 hours to give a yellow solution. The mixture was concentrated under reduced pressure to give a residue to give E39 (720 mg, crude) as a yellow gum.

General Schemes of Group F

[0309]
Procedure for Synthesis of F2

[0310] To a mixture of compound F1 (3 g, 16.20 mmol) and trimethylsilylformonitrile (1.61 g, 16.20 mmol, 2.03 mL) was added AlCl₃ (60 mg, 449.97 umol, 24.59 uL, 2.78e-2 eq), and the mixture was heated to 50° C. for 20 hours. TLC showed the reaction was completed. The reaction was quenched by water (10 mL) and then extracted with EtOAc (10 mL*2). The combined organic phase was dried over anhydrous Na₂SO₄, filtered and concentrated in vacuo to give the compound F2 (4.6 g) as a yellow solid.

Procedure for Synthesis of F3

[0311] To a solution of compound F2 (1 g, 3.52 mmol) in MeOH (10 mL) was added K₂CO₃ (52.48 mg, 379.71 umol). The mixture was stirred at 20° C. for 2 hr. TLC indicated that material was disappeared and one major new spot with larger polarity was detected. 8.75 mL of HCl (0.1 M) was added to the reaction mixture, and then it was extracted with EtOAc (2*20 mL). The combined organic layer was dried over (Na₂SO₄) and evaporated to dryness to give compound F3 (0.74 g) as yellow oil.

Procedure for Synthesis of F4

[0312] A mixture of compound F3 (2.42 g, 11.40 mmol), imidazole (993.59 mg, 14.59 mmol) and tert-butyl-chloro-dimethyl-silane (2.06 g, 13.68 mmol, 1.68 mL) in DMF (10 mL) was stirred at 20° C. for 14 hr. TLC indicated that material was consumed completely and new spots formed. The reaction mixture was diluted with water 50 mL and then it was extracted with EtOAc 100 mL (50 mL×2). The combined organic layers were washed with aqueous NaCl 100 mL (50 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica gel chromatography eluted with (PE:EtOAc=5:1) to give compound F4 (2.44 g) as colorless oil.

Procedure for Synthesis of F5

[0313] To the solution of compound F4 (1 g, 3.06 mmol) in THF (12 mL) was added LAH (200 mg, 5.27 mmol) at 0° C., and it was stirred at 0° C. for 0.5 hr to give a white suspension. TLC indicated that material disappeared. The reaction mixture was diluted with THF (20 mL) and then quenched with water (0.2 mL), 15% aq. NaOH (0.2 mL) and water (0.6 mL) at 0° C. Then it was stirred at 0° C. for 0.5 hr. The mixture was dried over anhydrous Na₂SO₄ and then filtered, and the filter cake was washed with EtOAc (20 mL). The combined filtrate was concentrated under reduced pressure to give compound F5 (870 mg, mixture of 2 trans-isomer) as colorless oil.

[0314]
Procedure for Synthesis of F7

[0315] To a mixture of F6 (1.7 g, 7.82 mmol), TEA (1.03 g, 10.2 mmol) in DCM (10 mL) was added TosCl (1.57 g, 8.21 mmol, 1.05) at 0° C. The reaction was stirred at 20° C. for 17 hours to give a yellow solution. LCMS showed the desired MS value was observed. The reaction was concentrated under reduced pressure. The concentrate was dissolved in EtOAc (150 mL) and the resulting solution was washed with aqueous HCl (100 mL, pH=4), aqueous NaOH (1 N, 100 mL), brine (150 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give F7 (2.49 g) as yellow oil.

Procedure for Synthesis of F8

[0316] To a mixture of F7 (2.3 g, 6.19 mmol) in DMSO (20 mL) was added KCN (443 mg, 6.81 mmol, 291 uL) and KI (1.54 g, 9.29 mmol), the mixture was stirred at 80° C. for 3 hours and 100° C. for 2 hours to give a black mixture. TLC showed the reactant was consumed. The reaction mixture was quenched with water (50 mL) and extracted with EtOAc (50 mL×2). The organic layer was washed with water (50 mL×2), brine (30 mL×4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford F8 (1.19 g) as a yellow oil.

Procedure for Synthesis of F9

[0317] A solution of F8 (600 mg, 2.65 mmol) in MeOH (20 mL) was added Raney-Ni (227 mg, 2.65 mmol), the suspension was degassed under vacuum and purged with H₂ several times, the mixture was stirred at 25° C. under H₂ (15 psi) for 16 hours to give a black mixture. TLC (PE/EA=1/1) showed the reaction was completed. The mixture was filtered and concentrated under reduced pressure to afford F9 (530 mg, crude) as a yellow oil.

[0318]
Procedure for synthesis of F11

[0319] To a mixture of F10 (1 g, 3.52 mmol) in THF (5 mL) was added N-methylmethanamine (2 M, 1.94 mL), the mixture was stirred at 25° C. for 1 hours to give a white mixture. TLC showed the new spot was observed. The mixture was concentrated under reduced pressure to give crude product. The crude product was poured into water (25 mL). The aqueous phase was extracted with DCM (15 mL×3). The combined organic phase was washed with brine (15 mL×4), dried with anhydrous Na₂SO₄, filtered and concentrated in vacuum to afford F11 (910 mg, 88.3% yield) as a white solid.

Procedure for Synthesis of F12

[0320] A mixture of F11 (400 mg, 1.37 mmol) in DCM (3 mL) and HCl/MeOH (3 mL) was stirred at 25° C. for 3 hours to give a white mixture. TLC showed the reaction was completed. The mixture was concentrated under reduced pressure to afford F12 (275 mg, 87.8% yield, HCl) as a white solid.

[0321]
Procedure for Synthesis of F14

[0322] Boc₂O (2.03 g, 9.29 mmol) was added to a stirred solution of F13 (1.00 g, 7.74 mmol) in THF (14 mL). The reaction was stirred at 25° C. for 17 hours to give a yellow solution. TLC showed the reaction was completed. The reaction was partitioned between EtOAc (80 mL) and H₂O (80 mL). The organic layer was washed with brine (80 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a yellow powder. The residue was treated with hexanes (30 mL) and the suspension was filtered and washed with hexane (5 mL×2). The filter cake was dried under reduced pressure to give F14 (1.26 g, 71% yield) as a white solid.

Procedure for Synthesis of F15

[0323] To a solution of F14 (1.84 g, 8.02 mmol) in THF (5 mL) and DCM (20 mL) were added TEA (3.65 g, 36.1 mmol) and TosCl (4.59 g, 24.1 mmol), DMAP (261 mg, 2.13 mmol) at 0° C. The mixture was then stirred at 25° C. for 17 hours to give a colorless solution. TLC showed the starting material was consumed completely. The mixture was partitioned between EtOAc (80 mL) and H₂O (80 mL). The organic layer was washed with brine (80 mL) and dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a white powder. The crude product was purified by combi flash to give F15 (2.91 g, 95% yield) as a white powder.

Procedure for Synthesis of F16

[0324] To a solution of F15 (1.76 g, 4.59 mmol) in DMSO (8 mL) was added acetylsulfanylpotassium (592 mg, 5.19 mmol). The reaction was stirred at 55° C. for 3 hours to give a yellow mixture. TLC showed the reaction was completed. After cooling, the reaction was quenched by adding saturated NaHCO₃ (32 mL). After stirring briefly, the solids that formed were filtered and washed with water (6 mL) to give a gray powder (2.7 g). The crude product was triturated with DCM/MeOH (10/1, 66 mL). The suspension was stirred at 25° C. for 30 min. After filtration, the filter cake was washed with EtOAc (10 mL). The filtration was concentrated under reduced pressure to give F16 (1.3 g, 99% yield) as a yellow powder.

Procedure for Synthesis of F17

[0325] To a mixture of F16 (0.66 g, 2.30 mmol) in AcOH (3 mL), H₂O (1.5 mL) and MeCN (9 mL) was added NCS (1.07 g, 8.04 mmol) at 0° C. The reaction was stirred at 25° C. for 25 min to give a yellow mixture. TLC showed the starting material was consumed completely. The mixture was partitioned between EtOAc (70 mL) and H₂O (70 mL). The organic extract was washed with brine (70 mL×2), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give yellow gum. The crude product was purified by combi flash to give F17 (350 mg, 49% yield) as a white powder.

Procedure for Synthesis of F18

[0326] A solution of F17 (350 mg, 1.12 mmol) in methanamine (5 mL) alcohol solution was stirred at 40° C. for 17 hours to give a yellow solution. TLC showed the starting material was consumed completely. The mixture was concentrated under reduced pressure to give F18 (340 mg, 99% yield) as a white powder.

Procedure for Synthesis of F19

[0327] To a solution of F18 (400 mg, 1.31 mmol) in DCM (4 mL) was added TFA (1 mL) at 0° C. The reaction was stirred at 25° C. for 1 hour to give a yellow solution. TLC showed the starting material was consumed completely. The mixture was concentrated under reduced pressure to give F19 (500 mg, crude) as yellow oil.

[0328]
Procedure for Synthesis of F21

[0329] To a mixture of F20 (2 g, 13.28 mmol, HCl) in THF (30 mL) and H₂O (15 mL) was added NaHCO₃ (3.35 g, 39.84 mmol) and Boc₂O (3.04 g, 13.94 mmol), the mixture was stirred at 25° C. for 16 hours to give a white mixture. TLC showed the new spot was observed. The mixture was quenched with water (20 mL) and extracted with EtOAc (20 mL×3). The organic was concentrated under reduced pressure to give a residue. The residue was purified by silica column to afford F21 (2.1 g, 9.80 mmol, 73.81% yield) as a white solid.

Procedure for Synthesis of F22

[0330] To a mixture of F21 (2.10 g, 9.80 mmol) in THF (40 mL) was added ZrCl₄ (5.71 g, 24.50 mmol) at −10° C., the mixture was stirred at −10° C. for 30 min. MeMgBr (3 M, 49.01 mL) was added, the mixture was stirred at 25° C. for 16 hours to give a white mixture. TLC showed the reactant was remained. The mixture was quenched with 30% NaOH solution (20 mL) and extracted with EtOAc (20 mL×3). The organic was concentrated under reduced pressure to give a residue. The residue was purified by silica column to afford F22 (510 mg, 2.23 mmol, 22.79% yield) as a yellow gum.

Procedure for Synthesis of F23

[0331] To a mixture of F22 (500 mg, 2.19 mmol) in THF (10 mL) and H₂O (5 mL) was added NaHCO₃ (367.92 mg, 4.38 mmol) and CbzCl (747.13 mg, 4.38 mmol) at 0-5° C., the mixture was stirred at 25° C. for 16 hours to give a yellow mixture. The reaction mixture was quenched by addition water 20 mL at 0° C., and then extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica column to afford F23 (850 mg, crude) as a colorless oil.

Procedure for Synthesis of F24

[0332] A solution of F23 (850.00 mg, 2.35 mmol) in HCl/MeOH (10 mL) was stirred at 0-10° C. for 1 hours to give a yellow mixture. The mixture was concentrated under reduced pressure to afford F24 (730 mg, crude) as a yellow oil.

[0333]
Procedure for Synthesis of F26

[0334] To a solution of F25 (1 g, 8.69 mmol) in DMSO (12 mL) was added NaH (1.04 g, 26.06 mmol, 60% purity) and bromomethylbenzene (4.46 g, 26.06 mmol). The mixture was stirred at 20° C. for 16 hr to give a white mixture. The mixture was quenched by saturated aqueous ammonium chloride (15 ml). The mixture was diluted with water 10 mL and extracted with Ethylacetate (40 mL*3). The combined organic layers were washed with brine (40 mL*3), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a yellow oil. The residue was purified by flash silica gel chromatography to give F26 (860 mg, 2.91 mmol, 33.52% yield) as a yellow oil.

Procedure for Synthesis of F27

[0335] A mixture of F26 (500 mg, 1.69 mmol), DTBMP (417.11 mg, 2.03 mmol) in DCM (30 mL) at −78° C. was added dropwise Tf₂O (573.11 mg, 2.03 mmol) under N₂, then, the mixture was stirred at −78° C. for 1 hr under N₂ atmosphere. MeMgBr (3 M, 1.69 mL) was added dropwise at −78° C. and the mixture was warmed to 20° C. The mixture was stirred at 20° C. for 2 hr to give a transparent mixture. The mixture was quenched by saturated aqueous ammonium chloride (15 ml). The mixture was diluted with water 10 mL and extracted with Ethylacetate (40 mL*3). The combined organic layers were washed with brine (40 mL*3), dried over Na₇SO₄, filtered and concentrated under reduced pressure to give a yellow oil. The residue was purified by flash silica gel chromatography to give F27 (420 mg, 1.36 mmol, 80.18% yield) as a yellow oil.

Procedure for Synthesis of F28

[0336] To a solution of F27 (420 mg, 1.36 mmol) in MeOH (15 mL) was added Boc₂O (592.44 mg, 2.71 mmol) and wet Pd(OH)₂/C (100 mg) under N₂ atmosphere. The suspension was degassed and purged with H₂ 2 times. The mixture was stirred under H₂ (15 Psi) at 20 C for 16 hr to give a black mixture. The reaction mixture was filtered and concentrated under reduced pressure to give a yellow oil. The residue was dissolved with MeOH (20 mL) and KOH (151 mg) was added. The mixture was stirred at 20° C. for 1 hr. The reaction mixture was concentrated under reduced pressure to give yellow oil. Then the residue was diluted into water (20 mL) extracted with EtOAc (20 mL×3). The combined extracts were washed with brine (20 mL*2), dried over Na₂SO₄ and concentrated under reduced pressure to give F28 (460 mg, crude) as a yellow oil.

Procedure for Synthesis of F29

[0337] To a solution of F28 (460 mg, 1.44 mmol) in MeOH (15 mL) was added wet Pd(OH)₂/C (100 mg) under N₂ atmosphere. The suspension was degassed and purged with H₂ 2 times. The mixture was stirred under H₂ (15 Psi) at 20° C. for 16 hr to give a black mixture. LC-MS showed the desired compound was not detected. The mixture was stirred under H₂ (15 Psi) at 20° C. for 64 hr to give a black mixture. The reaction mixture was filtered and concentrated under reduced pressure to give a yellow oil. The residue was purified by flash silica gel chromatography to give F29 (190 mg, 828.55 umol, 57.54% yield) as a white solid.

[0338] Commercial available reagents were used for group F such as benzyl piperidin-4-ylcarbamate, tert-butyl piperidin-4-ylcarbamate, tert-butyl piperazine-1-carboxylate, tert-butyl 2-(aminomethyl)morpholine-4-carboxylate, tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate, tert-butyl 4-aminopiperidine-1-carboxylate, 4-methoxypiperidine, piperidin-4-ylmethanamine, 4-methoxycyclohexan-1-amine, (tetrahydro-2H-pyran-4-yl)methanamine, morpholine, azepan-4-ol, pyrrolidin-3-ol, 4-aminocyclohexan-1-ol, N-methylpiperidin-4-amine, (1R, 4R)-4-(aminomethyl)cyclohexan-1-ol, (1S, 3S)-3-aminocyclopentan-1-ol, piperidin-4-ol, 4-(aminomethyl)piperidin-2-one, piperidin-4-ylmethanol, 4-(trifluoromethoxy)piperidine, 4-ethoxypiperidine, 4-isopropoxypiperidine, 4-ethoxycyclohexan-1-amine, 4-methoxycyclohexan-1-amine, (3R,4R)-4-(aminomethyl)piperidin-3-ol, (3S,4S)-4-(aminomethyl)piperidin-3-oland 4-isopropoxycyclohexan-1-amine, (3R,4S)-4-(aminomethyl)piperidin-3-ol, (3S,4R)-4-(aminomethyl)piperidin-3-ol and 3-aminopropan-1-ol.

[0339]

[0340] The method to prepare compounds of formula V-5 and V-6 is shown in Scheme 20.

[0341] Route V: Compound G3 can be treated with NaOEt to give compounds I1. Compound I1 can be treated with POCl₃ to give compounds I2. Compound I2 can be treated with group E in presence of DIPEA to give compounds V-1. Compound V-1 can be treated with Boc₂O to give compounds V-2. Compound V-2 can be treated with group F in presence of Pd₂(dba)₃ to give compounds V-3. Compound V-3 can be treated with Pd/C and H₂, or HCl to give compounds V-4. Compound V-4 can be treated with group C which was defined claim 1 to give compounds V-5. Compounds V-5 can be treated with acid such as HCl to obtain the compounds of formula V-6.

Procedure for Synthesis of I1

[0342] Na (790 mg, 34.3 mmol) was added into anhydrous EtOH (125 mL), the mixture was stirred at 10° C. for an hour. Compound G3 (3.50 g, 27.9 mmol) and diethyl propanedioate (5.42 g, 33.8 mmol) were added into this solution. The mixture was stirred at 78° C. for 16 hours under N₂ atmosphere to give a yellow solution. TLC showed the reaction was completed. The mixture was concentrated under reduced pressure. The residue was dissolved in water (60 mL) and acidified to pH=3 with 3M HCl, then filtered to give compound I1 (3.70 g) as a white powder.

Procedure for synthesis of I2

[0343] To a mixture of compound I1 (1.30 g, 6.73 mmol) in POCl₃ (20.6 g, 134 mmol) was added N,N-diethylaniline (672 mg, 4.51 mmol). The mixture was stirred at 100° C. for 16 hours under 1\1, atmosphere. TLC showed a new spot. Most of POCl₃ was removed under reduced pressure. Then the mixture was poured into H₂O (40 mL), extracted with DCM (50 mL×3). The organic layer was washed with brine (50 mL×2), dried over anhydrous Na₂SO₄, then filtered, and concentrated under reduced pressure to give compound I2 (3.11 g, crude) as a yellow oil, without further purification for next step.

[0344]

[0345] The method to prepare compounds of formula VI-5 is shown in Scheme 28.

[0346] Route VI: Compound G3 can be treated with X-substituted acetoacetate and acetic acid to give compounds VI-1. Compound VI-1 can be treated with POCl₃ to give compounds VI-2. Compound VI-2 can be treated with group E in presence of DIPEA to give compounds VI-3. Compound VI-3 can be treated with Pd/C and H₂ to give compounds VI-4. Compound VI-4 can be treated with group C which was defined claim 1 to give compounds VI-5.

[0347]
Procedure for Synthesis of G2

[0348] To a mixture of diisopropylamine (6.69 g, 66.2 mmol) in anhydrous THF (20 mL) was added n-BuLi (2.5 M, 27.7 mL) at 0° C. and stirred at 0° C. for 0.5 hour, then the mixture was cooled to −70° C. and G1 (5.00 g, 60.2 mmol) in THF (20 mL) was added into the mixture at −70° C. and stirred at −70° C. for 0.5 hour, then the mixture was poured into a mixture of ethyl formate (4.90 g, 66.2 mmol) in THF (20 mL) at −70° C. under N, atmosphere and the resulting mixture was stirred at −70° C. for 0.5 hours, then warmed to 15° C. and stirred at 15° C. for 17 hours. TLC (silica gel, PE/EtOAc=2/1) showed the reaction was completed. The reaction mixture was poured into aqueous HCl (150 mL, 1M) at 0° C. and stirred at 0° C. for 0.5 hours, then the mixture was extracted with EtOAc (150 mL×3). The organic layer was washed with brine (250 ml), dried over anhydrous Na₂SO₄, filtered, the filtrate was concentrated under reduced pressure to give compound G2 (5.0 g) as a yellow oil. The crude product was used directly in next step without further purification.

Procedure for Synthesis of G3

[0349] To a solution of compound G2 (8.82 g, 67.5 mmol) and AcOH (7.09 g, 118 mmol) in EtOH (5 mL) was added NH₂—NH₂·H₂O (4.39 g, 87.7 mmol), the resulting mixture was stirred at 78° C. for 17 hours to give a pale yellow solution. TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give a residue, then the pH value of the residue was adjusted to 9 with aqueous NaOH (1M), diluted with water (50 mL) and extracted with EtOAc (100 mL×3). The organic layer was washed with brine (150 mL), dried over anhydrous Na₂SO₄, filtered and the filtrate was concentrated under reduced pressure to give compound G3 (10.0 g, crude) as a yellow gum. The crude product was used directly in next step without further purification.

Procedure for Synthesis of G4

[0350] To a mixture of compound G3 (5.00 g, 40.0 mmol) in anhydrous DCM (25 mL) was added a mixture of ethoxycarbonyl isothiocyanate (4.72 g, 36.0 mmol) in anhydrous DCM (25 mL) at −70° C. and stirred at −70° C. for 1 hour, a lot of white solid appeared. TLC showed the reaction was completed. Then the mixture was allowed to warm to −10° C. and filtered, and the filter cake was washed with DCM (15 mL) to give 4.50 g of desired compound as a white solid, the structure was confirmed by HNMR. The filtrate was purified by silica gel column to give compound G4 (1.80 g) as a white solid.

Procedure for Synthesis of G5

[0351] To a mixture of compound G4 (6.30 g, 24.6 mmol) in MeCN (50 mL) was added K₂CO₃ (6.79 g, 49.2 mmol), the mixture was stirred at 80° C. for 8 hours. Crude LCMS showed the reaction was completed. The mixture was cooled to room temperature, then AcOH (15 mL) was added into the mixture and stirred at 15° C. for 20 minutes, then the resulting mixture was concentrated under reduced pressure to give a residue, which was washed with water (50 mL×3) to give compound G5 (4.20 g) as a white solid.

Procedure for Synthesis of G6

[0352] To a mixture of compound G5 (4.20 g, 20.0 mmol) in EtOH (40 mL) was added NaOH (2.00 g, 50.0 mmol) in H₂O (20 mL) at 15° C., then Mel (2.84 g, 20.0 mmol) was added into above mixture and the resulting mixture was stirred at 15° C. for 2 hours. Crude LCMS showed the reaction was completed. The mixture was concentrated under reduced to give a residue, which was treated with ice cold water (50 mL) and aqueous HCl (20 mL, 6M) for 30 minutes, a lot of white solid appeared, filtered to give the crude product. The crude product was poured into MeCN (50 mL) to give a suspension, then the suspension was concentrated under reduced pressure to give compound G6 (3.60 g) as a white solid.

Procedure for Synthesis of G7

[0353] To a mixture of compound G6 (1.00 g, 4.46 mmol) in DCM (30 mL) was added m-CPBA (3.07 g, 14.2 mmol) in portions at 20° C. The reaction mixture was stirred at 20° C. for 2 hours. LCMS showed the reaction was complete. The reaction mixture was diluted with a mixture solution of brine (20 mL) and NaOH/H₂O (3M, 10 mL). The aqueous layer was separated and brought pH to 1 with HCl (3M). A lot of white powder was precipitated. The mixture was then extracted with EtOAc (50 mL×2). The organic layer was washed with brine (20 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give a residue. The residue was purified by Combi Flash to give compound G7 (1.03 g) as light brown gum.

Procedure for Synthesis of G9

[0354] To a solution of compound G7 (6.62 g, 25.83 mmol) in NMP (100 mL) was added compound G8 (18.15 g, 77.5 mmol). The reaction mixture was stirred at 140° C. for 16 hours. TLC showed the reaction was complete. The reaction mixture was partitioned between brine (500 mL) and EtOAc (400 mL). The organic layer was washed with water (100 mL×2), brine (100 mL), dried over anhydrous Na₂SO₄, and concentrated under reduced pressure to give a residue. The residue was purified by Combi Flash to give a brown gum, which was triturated with CH₃CN (50 mL) to give compound G9 (2.06 g) as an off-white powder.

Procedure for Synthesis of G10

[0355] To a mixture of compound G9 (89 mg, 0.22 mmol) in POCl₃ (4.41 g, 28.7 mmol) was added N,N-diethylaniline (97 mg, 0.65 mmol) at 20° C. The reaction mixture was stirred at 80° C. for 2 hours. The reaction mixture was concentrated under reduced pressure to give compound G10 (93 mg) as an brown gum as the crude product. The crude product was used directly in next step without further purification.

Procedure for Synthesis of G11

[0356] To a solution of compound G10 (127 mg, 0.297 mmol), DIPEA (95.9 mg, 0.742 mmol) in DMF (2 mL) was added compound A7 (131 mg, 0.371 mmol). The reaction solution was stirred at 10° C. for 1 hour. LCMS showed the desired MS value. The reaction mixture was partitioned between EtOAc (20 mL) and saturated aqueous NaHCO₃ solution (20 mL). The organic layer was washed with brine (10 mL), dried over anhydrous Na₇SO₄, filtered, concentrated under reduced pressure. The residue was purified by Combi flash to give compound G11 (103 mg) as a brown gum

Procedure for Synthesis of Compound 1

[0357] To a solution of compound G11 (70 mg, 0.094 mmol) in AcOH (0.5 mL) was added HBr/AcOH (0.5 mL, 35% purity) at 15° C. This reaction solution was stirred at 15° C. for 1 hour to give a light brown solution. LCMS showed the reaction was complete. The reaction was diluted with 5 mL of MTBE to precipitate a grey powder, which was collected by filtration. The solid was dissolved in MeOH (4 mL), and then a drop of ammonia water (28%) was added to basify the solution. The crude product dissolved in MeOH was purified by prep-HPLC. The eluent containing the desired product was concentrated under reduced pressure and the residual solution was lyophilized to give compound 1 (9.9 mg) as a white powder.

[0358]
Procedure for Synthesis of G12

[0359] To a solution of compound A23 (183 mg, 0.385 mmol) in CH₃CN (10 mL) was added DIPEA (226 mg, 1.75 mmol) and compound G10 (150 mg, 0.35 mmol). The resulting mixture was stirred at 20° C. for 1 hour to give white suspension. TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (10 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to obtain compound G12 (75 mg) as an off-white solid.

Procedure for Synthesis of Compound 9

[0360] A solution of compound G12 (30 mg, 0.4 mmol) in HBr/HOAC (35%) (1 mL) was stirred at 20° C. for 1 hour to give yellow solution. TLC showed the reaction was completed. The reaction was addition MTBE (50 mL) and lots of solid was precipitated, filtered under reduced pressure to give filter cake as an off-white solid. The filter cake was purified by prep-HPLC. The residue was concentrated most of solvent and lyophilized to obtain compound 9 (7.8 mg) as a white powder.

[0361]
Procedure for Synthesis of G13

[0362] A solution of compound B11 (50 mg, 0.2 mmol) and compound G10 (90 mg, 0.2 mmol) in CH₃CN (5 mL) was added DIPEA (27.1 mg, 0.2 mmol). The resulting mixture was stirred at 0° C. for 30 min to give red solution. TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to obtain compound G13 (100 mg) as a yellowish solid.

Procedure for Synthesis of G14

[0363] To a solution of compound G13 (100 mg, 0.158 mmol) in THF (5 mL) was added compound A5 (58.2 mg, 0.317 mmol) and DIPEA (82 mg, 0.634 mmol), the resulting mixture was stirred at 20° C. for 1 hour to give red solution, LCMS showed the reaction was completed, dimethylamine (71.5 mg, 1.59 mmol) was added to the mixture, then stirred for another 3 hours at 20° C. to give red solution. TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to give 100 mg (impure), which was purified by prep-TLC to obtain compound G14 (50 mg) as a yellow solid.

Procedure for Synthesis of Compound 16

[0364] A solution of compound G14 (50 mg, 67.4 umol) in HBr/HOAc (35%) (1 mL) was stirred at 20° C. for 30 min to give red solution. LCMS showed the reaction was completed. To the reaction mixture was added MTBE (3 mL) to precipitate a yellow gum. The yellow gum was collected by filtration and washed with MTBE (3 mL×2). The yellow gum was dissolved in MeOH (2 mL) and purified by cation exchange resin eluting with 5% NH₃·H₂O/MeOH, then lyophilized to obtain compound 16 (29.9 mg) as a yellow solid.

[0365]
Procedure for Synthesis of G15

[0366] To a mixture of compound B17 (403 mg, 0.866 mmol) in MeCN (5 mL) was added DIPEA (976 uL), compound G10 (338 mg, 0.787 mmol). The mixture was stirred at 15° C. for 0.5 hour to give a yellow mixture. TLC showed the reaction was completed. The mixture was partitioned between DCM (50 mL) and water (50 mL), the mixture was extracted with DCM (50 mL×2), the combined extracted was washed with brine (50 mL), dried over Na₂SO₄, filtered, concentrated under reduced pressure to give a yellow oil, which was purified by Combi flash to give compound G15 (250 mg) as yellow oil.

Procedure for Synthesis of G16

[0367] To a mixture of compound G15 (250 mg, 0.397 mmol) in THF (5 mL) was added DIPEA (0.257 mg, 1.98 mmol), compound A5 (218 mg, 1.19 mmol). The yellow mixture was stirred at 15° C. for 1 hour. The color of mixture was become black. LCMS showed the reaction was completed. Dimethylamine (2 M, 992 uL) was added to the mixture and stirred at 15° C. for 1 hour to give a black brown mixture. LCMS showed the reaction was completed. The mixture was partitioned between DCM (50 mL) and water (30 mL), The aqueous was extracted with DCM (50 mL×2), the combined extracted phase was washed with brine (30 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give a brown oil, which was purified by Combi flash to give compound G16 (250 mg) as a brown gum.

Procedure for Synthesis of Compound 25

[0368] A mixture of compound G16 (250 mg, 0.337 mmol) in HBr/HOAc (3 mL) was stirred at 15° C. for 0.5 hour to give a yellow mixture. LCMS showed the reaction was complete. To the reaction mixture was added MTBE (10 mL) to precipitate yellow powder. The white powder was collected by filtration and washed with MTBE (5 mL×2), basified by saturated Na₂CO₃ to pH=9-10, and extracted with DCM (50 mL×2), the combined organic phase was washed with water (50 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give yellow oil, which was purified by prep-HPLC (0.1% TFA), basified by saturated Na₂CO₃ to pH=9-10, and extracted with DCM (50 mL×3), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give compound 25 (30 mg) as a white powder.

[0369]
Procedure for Synthesis of G17

[0370] To a solution of compound B23 (230 mg, 0.633 mmol) in CH₃CN (5 mL) was added DIPEA (818 mg, 6.33 mmol) and compound G10 (299 mg, 0.696 mmol) at 0-5° C. The reaction was stirred at 25° C. for 1 hour to give a black brown solution. LCMS showed desired MS value. The reaction was diluted with DCM (30 mL) and concentrated under reduced pressure. The residue was partitioned between water (50 mL) and DCM (100 mL). The separated organic layer was washed with water (80 mL), brine (80 mL), dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound G17 (150 mg) as yellow oil.

Procedure for Synthesis of G18

[0371] To a solution of compound G17 (200 mg, 0.312 mmol) in THF (5 mL) was added DIPEA (201 mg, 1.56 mmol) and compound A5 (172 mg, 0.935 mmol). The reaction solution was stirred at 25° C. for 30 minutes to give a black brown solution. Then, dimethylamine (2 M, 1.56 mL) was added and stirred for another 16 hours to give a black brown solution LCMS and TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure. The residue was partitioned between DCM (150 mL) and water (100 mL). The organic layer was washed with water (100 mL), brine (100 mL) and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound G18 (100 mg) as a yellow oil.

Procedure for Synthesis of Compound 20

[0372] A solution of compound G18 (150 mg, 0.199 mmol) in HBr/HOAc (2 mL, 35%) was stirred at 25° C. for 0.5 hour to give a red solution. LCMS showed the reaction was completed. 10 mL MTBE was added and the resulting white mixture was filtered. The filter cake was collected, washed with MTBE (20 mL), dissolved in MeOH (3 mL) and basified by cation exchange resin to give compound 20 (46.6 mg) as a yellow powder.

[0373]
Procedure for Synthesis of G19

[0374] To a solution of compound B31 (400 mg, 0.933 mmol) in CH₃CN (10 mL) was added DIPEA (362 mg, 2.80 mmol) and compound G10 (500 mg, 1.38 mmol) at 0-10° C. The reaction was stirred for 1 hour at 25° C. to give a brown solution. Crude LCMS showed the reaction was completed. TLC showed new spot formed. The reaction solution was concentrated under reduced pressure. The residue was purified by Combi Flash to give compound F19 (380 mg) as a yellow gum.

Procedure for Synthesis of G20

[0375] To a solution of compound G19 (380 mg, 0.600 mmol) in THF (5 mL) was added a solution of compound A5 (330 mg, 1.80 mmol) in THF (2 mL) at 0-5° C. in an ice-bath. The reaction solution was stirred at 0-25° C. for 0.5 hour. Dimethylamine (2M, 3 mL, 10 eq) was added and stirred for another 2 hours to give a black brown solution. Crude LCMS showed the reaction was completed. TLC showed the reaction was completed. The reaction solution was concentrated under reduced pressure. The residue was dissolved in DCM (200 mL), washed with saturated NH₄Cl (100 mL), water (100 mL) and brine (100 mL), the organic layer was dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by Combi Flash to give compound G20 (130 mg) as a yellow solid.

Procedure for Synthesis of Compound 11

[0376] A solution of compound G20 (70 mg, 0.093 mmol) in HBr/HOAc (1 mL, 35%) was stirred at 25° C. for 0.5 hour to give a yellow solution. LCMS showed desired MS value. 10 mL MTBE was added and the resulting mixture was filtered to give a white solid. The solid was dissolved in MeOH (2 mL), purified by cation exchange resin and lyophilized to give a white powder which was further purified by prep-HPLC. The fraction was concentrated under reduced pressure. The residue was neutralized to pH=7-8 with K₂CO₃ (solid). The resulting white mixture was extracted with EtOAc (50 mL×2). The organic layer was dried over anhydrous Na₂SO₄, concentrated and lyophilized to give compound 11 (23.1 mg) as a white powder

[0377]
Procedure for Synthesis of G21

[0378] To a solution of compound D3 (300 mg, 0.7 mmol) and compound G10 (448 mg, 1.40 mmol) in CH₃CN (20 mL) was added DIPEA (181 mg, 1.40 mmol). The resulting mixture was stirred at 20° C. for 1 hour to give yellow solution. LCMS showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give a residue, TLC. The residue was purified by Combi flash to compound G21 (240 mg) as a yellow oil.

Procedure for Synthesis of G22

[0379] To a solution of compound G21 (240 mg, 0.34 mmol) in DCM (7 mL) was added TFA (4.62 g, 40.5 mmol). The resulting mixture was stirred at 20° C. for 1 hour to give yellow solution. TLC and LCMS showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give compound G22 (268 mg) as a yellow oil.

Procedure for Synthesis of G23

[0380] To a solution of compound G22 (268 mg, 0.37 mmol) in THF (20 mL) was added DIPEA (143 mg) and compound A5 (67.6 mg, 0.37 mmol), the resulting mixture was stirred at 20° C. for 1 hour, LCMS showed the reaction was completed, then dimethylamine (83.1 mg, 1.84 mmol) was added to the mixture and stirred for another 2 hours to give yellow suspension. TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL), extracted with EtOAc (50 mL). The organic layers were washed with brine (20 mL), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by Combi flash to give compound G23 (74 mg) as a yellow oil.

Procedure for Synthesis of Compound 18

[0381] A solution of compound G23 (74.0 mg, 0.1 mmol) in HBr/HOAc (35%) (1 mL) was stirred at 20° C. for 1 hour to give yellow solution. LCMS showed the reaction was completed. To the reaction mixture was added MTBE (3 mL) to precipitate a white gum. The gum solid was collected by filtration and washed with MTBE (3 mL×2). The white gum was dissolved in MeOH (2 mL) and purified by cation exchange resin (PCX-SPE) eluting with 5% NH₃·H₂O/MeOH, the flows was concentrated and lyophilized to obtain compound 18 (42.9 mg) as a white powder.

[0382]
Procedure for Synthesis of G24

[0383] To a mixture of compound G6 (1.00 g, 4.46 mmol) in POCl₃ (14 mL) was added N,N-diethylaniline (2.00 g, 13.4 mmol) at 15° C., the mixture was stirred at 90° C. for 3 hours. The mixture was concentrated under reduced pressure to give compound G24 (3.20 g, crude) as a brown gum, which was used to next step without purification.

Procedure for Synthesis of G25

[0384] To a solution of MO (7.32 g, 26.2 mmol) in MeCN (70 mL) was added DIEA (6.77 g, 52.4 mmol, 9.13 mL), G24 (6.36 g, 26.2 mmol). The reaction mixture was stirred at 25° C. for 16 hours to give brown mixture. TLC showed new spot. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL*2). The organic layer was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to give G25 (11.3 g) as yellow solid.

Procedure for Synthesis of G26

[0385] To a mixture of G25 (11.3 g, 23.2 mmol) in DCM (110 mL) was added m-CPBA (10.0 g, 46.5 mmol, 80% purity) at 0-10° C., the mixture was stirred at 0-10° C. for 2 hours to give a yellow mixture. LCMS showed the reaction was not completed. The mixture was stirred at 0-10° C. for another 1 hour to give a yellow mixture. LCMS showed the desired product was observed. The mixture was partitioned between DCM (100 mL) and saturated aqueous Na₂SO₂ (100 mL). The aqueous phase was extracted with DCM (100 mL×2). The combined organic extract was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford G26 (6.6 g) as a yellow solid.

Procedure for Synthesis of G27

[0386] To a solution of 4-methoxycyclohexanamine (71.9 mg, 0.556 mmol) and G26 (180 mg, 0.348 mmol) in NMP (1 mL) was added DIEA (135 mg, 1.04 mmol). The resulting mixture was heated at 110° C. and stirred for 12 hrs to give brown solution. LCMS and TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (30 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO₂, Petroleum ether/Ethyl acetate=1:1) to obtain compound G27 (105 mg) as an orange yellow solid.

Procedure for Synthesis of G28

[0387] The compound G27 (105 mg) was followed the same procedure of B7 to obtain 110 mg of compound G28 as a yellow solid.

Procedure for Synthesis of Compound 44

[0388] To a solution of G28 (110 mg, 0.172 mmol) in NMP (2 mL) was added (E)-4-(dimethylamino)but-2-enoyl chloride (3 M, 172 uL) at 0° C., the resulting mixture was stirred at 15° C. for 12 hour to give yellow solution, LCMS showed most of the starting material consumed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC, then concentrated to obtain compound 44 (21 mg) as a light yellow solid.

[0389]
Procedure for Synthesis of G29

[0390] To a solution of compound G26 (300 mg, 0.58 mmol) and tert-butyl piperazine-1-carboxylate (323.88 mg, 1.74 mmol) in NMP (3 mL) was added DIPEA (149.83 mg, 1.16 mmol, 201.93 uL). The resulting mixture was heated at 110° C. and stirred for 2 hrs to give yellow solution. LCMS and TLC showed the reaction was completed. The reaction mixture was quenched by addition H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (30 mL×3), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to obtain compound G29 (285 mg) as a yellow solid.

Procedure for Synthesis of G30

[0391] The compound G29 (285 mg) was followed the same procedure of B7 to obtain 258 mg of compound G30 as a yellow solid.

Procedure for Synthesis of G31

[0392] To a solution of 2-fluoroprop-2-enoic acid (16.38 mg, 181.90 umol) in DMF (2 mL) were added TEA (46.02 mg, 454.76 umol, 63.30 uL) and HATU (69.17 mg, 181.90 umol), and then compound G30 (90 mg, 151.59 umol) was added to the mixture and stirred at 15° C. for 2 hours to give brown solution. LCMS showed part of the starting material remained, the reaction was stirred at 15° C. for another 2 hours to give brown solution. LCMS indicated that the reaction was almost complete. The reaction mixture was poured into water (15 mL), and the yellow suspension was filtered. The filter cake was washed with PE (10 mL) and dried to give compound G31 (100 mg) as a yellow solid.

Procedure for Synthesis of Compound 79

[0393] A mixture of compound G31 (100 mg) in 4M HCl/MeOH (2 mL) was stirred at 15° C. for 1 hr to give a yellow solution. LCMS and HPLC indicated that the reaction worked well. The solvent was removed under reduced pressure to give the crude product. It was purified by prep-HPLC most of solvent was removed under reduced pressure, and the remaining solvent was removed by lyophilization to give compound 79 (34.7 mg) as a yellow solid.

[0394]
Procedure for Synthesis of G32

[0395] To a mixture of compound G26 (500 mg, 0.96 mmol) and tert-butyl N-(4-piperidyl)carbamate (386 mg, 1.93 mmol) in NMP (5 mL) was added DIEA (249 mg, 1.93 mmol, 336 uL), and the mixture was stirred at 110° C. for 16 hours to give a brown mixture. LCMS showed the reaction was completed. The reaction mixture was quenched with water (20 mL) and extracted with EtOAc (20 mL×2). The organic layer was washed with water (20 mL×2), brine (30 mL×4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford compound G32 (520 mg) as a red solid.

Procedure for Synthesis of G33

[0396] The compound G32 (520 mg) was followed the same procedure of B7 to obtain 450 mg of compound G33 as a yellow solid.

Procedure for Synthesis of G34

[0397] To a solution of compound G33 (50 mg, 82 umol, 1 eq) in THF (2 mL) was added a solution of A5 (30 mg, 164 umol, 2 eq) in THF (2 mL) at 0-5° C. in an ice-bath. The reaction solution was stirred at 0-25° C. for 1.5 hours. 2-(methylamino)acetamide (21 mg, 246 umol, 3 eq) and DIEA (10 mg, 82 umol, 14 uL, 1 eq) were added and it was stirred for another 16 hours to give a black brown solution. LCMS showed the desired product was observed. The reaction mixture was quenched with water (20 mL) and extracted with EtOAc (20 mL×2). The organic layer was washed with water (20 mL×2), brine (30 mL×4), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by prep-TLC to afford compound G34 (22 mg) as a white powder.

Procedure for Synthesis of Compound 58

[0398] The compound G34 (22 mg) was followed the same procedure of compound 79 to obtain 3 mg of compound 58 as a yellow solid.

[0399]
Procedure for Synthesis of G35

[0400] To a solution of compound EN (728 mg, 2.61 mmol) and compound 12 (500 mg, 2.17 mmol) in EtOH (10 mL) was added DIPEA (561 mg, 4.35 mmol, 0.757 mL, 2 eq). The resulting mixture was stirred at 75° C. for 12 hrs to give brown solution. TLC showed the reaction was completed. The reaction mixture was concentrated under reduced pressure to give a residue. Then diluted with H₂O (50 mL) and extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (20 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to obtain compound G35 (948 mg) as a brown gum.

Procedure for Synthesis of G36

[0401] The compound G35 (948 mg) was followed the same procedure of compound B14 to obtain 930 mg of compound G36 as a yellow solid.

Procedure for Synthesis of G38

[0402] To a mixture of compound G36 (200 mg, 349 umol) and compound G37 (90.19 mg, 698 umol) in toluene (5 mL) were added Pd₂(dba); (31.9 mg, 34.9 umol), t-BuONa (50.3 mg, 523 umol, 1.5 eq) and BINAP (21.7 mg, 34.9 umol), and the mixture was stirred at 95° C. for 4 hours to give a yellow mixture. LCMS showed the reaction was not completed. The mixture was stirred at 95° C. for another 6 hours to give a red mixture. TLC showed the reaction was completed. The mixture was partitioned between EtOAc (15 ml) and water (10 mL). The aqueous phase was extracted with EtOAc (10 mL×2). The combined organic extract was washed with brine (130 mL), dried over Na₂SO₄, filtered, concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford compound G38 (130 mg) as a yellow solid.

Procedure for Synthesis of G39

[0403] The compound G38 (130 mg) was followed the same procedure of compound B7 to obtain 110 mg of compound G39 as a yellow solid.

Procedure for Synthesis of G40

[0404] The compound G39 (100 mg) was followed the same procedure of compound G31 to obtain 70 mg of compound G40 as a yellow solid.

Procedure for Synthesis of Compound 81

[0405] The compound G40 (70 mg) was followed the same procedure of compound 79 to obtain 18 mg of compound 81 as a yellow solid.

[0406]
Procedure for Synthesis of G41

[0407] To a mixture of G3 (1 g, 7.99 mmol) into acetic acid (10 mL) was added ethyl acetoacetate (1.30 g, 9.99 mmol, 1.26 mL). The mixture was heated to 110-115° C. and stirred for 12 hr to give a yellow mixture. LCMS showed the reaction was completed. The mixture was added PE (30 mL) and filtered, the filter cake was dried to afford product G41 (800 mg, 4.18 mmol, 52.37% yield) as a yellow solid.

Procedure for Synthesis of G42

[0408] A suspension of G41 (800 mg, 4.18 mmol, 1 eq) and N,N-DIMETHYLAMINE (329.52 mg, 2.72 mmol, 344.68 uL, 0.65 eq) in MeCN (5 mL) was heated to 50-55° C. Then POCl₃ (1.60 g, 10.46 mmol, 971.91 uL, 2.5 eq) was added dropwise and the resulting mixture was heated to 60-65° C. for 9 hours to give a red mixture. TLC showed the reaction was completed. The mixture was concentrated under reduced pressure to give a residue. The residue was purified by silica gel chromatography to afford G42 (400 mg, 1.91 mmol, 45.6% yield) as a white solid.

Procedure for Synthesis of G43

[0409] To a mixture of E10 (1.60 g, 2.86 mmol, 1.5 eq) in CH₃CN (10 mL) was added DIEA (493.12 mg, 3.82 mmol, 664.58 uL, 2 eq) and G42 (400 mg, 1.91 mmol, 1 eq), the mixture was stirred at 60° C. for 48 hours to give a black mixture. LCMS showed the desired product was observed. The mixture was partitioned between EtOAc (30 mL) and H₂O (20 mL). The aqueous phase was extracted with EtOAc (30 mL×2). The combined organic extract was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The crude product was purified by combi flash to afford G43 (1.5 g, crude) as a yellow gum.

Procedure for Synthesis of G44

[0410] The compound G43 (1.5 g) was followed the same procedure of compound B7 to obtain 740 mg of compound G44 as a yellow solid.

Procedure for Synthesis of Compound 153

[0411] The compound G44 (300 mg) was followed the same procedure of compound G23 to obtain 40 mg of compound 153 as a brown powder.

[0412]
Procedure for Synthesis of G45

[0413] To a solution of E39 (720 mg, 1.48 mmol, 1 eq) in CH₃CN (10 mL) was added DIEA (381.78 mg, 2.95 mmol, 514.53 uL, 2 eq) and G24 (358.51 mg, 1.48 mmol), the mixture was stirred at 15° C. for 1 hour to give a yellow mixture. The mixture was partitioned between EtOAc (30 mL) and H₂O (30 mL). The aqueous phase was extracted with EtOAc (30 mL×2). The combined organic extract was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure. The crude product was purified by silica column to afford G45 (580 mg, 1.00 mmol, 67.74% yield) as a yellow gum.

Procedure for Synthesis of G46

[0414] To a solution of G45 (330 mg, 569.25 umol) in THF (6 mL), MeOH (3 mL) and H₂O (3 mL) was added Oxone (349.96 mg, 569.25 umol) at 0-5° C., the mixture was stirred at 0-5° C. for 2 hours. The mixture was treated with additional 0.5 eq Oxone (285 mg). The mixture was stirred at 0-5° C. for another 1 hour to give a yellow mixture. The mixture was added to another 0.5 eq Oxone (285 mg), the mixture was stirred at 0-5° C. for another 5 hours to give a yellow mixture. The mixture was quenched by saturated Na₂CO₃ (10 mL) and then partitioned between EtOAc (30 mL) and H₂O (30 mL). The aqueous phase was extracted with EtOAc (30 mL×2). The combined organic extract was dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give a crude product. The crude product was purified by silica column to afford G46 (220 mg, 359.65 umol, 63.18% yield) as an off-white solid.

Procedure for Synthesis of G47

[0415] To a solution of E39 (71.98 mg, 313.87 umol) in THF (2 mL) was treated with NaH (14.12 mg, 353.11 umol, 60% purity) at 20° C., then, heated to 50° C. At 50° C., a solution of G46 in DMF (0.5 mL) was added drop-wise. After addition, the reaction mixture was heated at 50° C. for 1.5 h to give pale yellow mixture. The reaction was cooled to 0° C., quenched with water (10 mL), diluted with EA (20 mL). The organic layer was washed with water (10 mL×3). The combined organic layer was dried over Na₂SO₄, concentrated in vacuum to give crude oil. The crude oil was purified by prep-TLC to give G47 (160 mg, 210.27 umol, 76.56% yield) as pale yellow gum.

Procedure for Synthesis of G48

[0416] To a solution of G47 (170 mg, 223.41 umol, 1 eq) in THF (6 mL) was Pd/C (60 mg, 22.34 umol, 10% purity, 0.1 eq), the mixture was stirred at 25° C. under H₂ atmosphere for 16 hours to give a black mixture. The reaction mixture was filtered and concentrated under reduced pressure to give a residue (170 mg). The part of residue (60 mg) was purified by prep-TLC to afford G48 971-9 (30 mg, 46.57 umol, 20.85% yield) as a white powder.

Procedure for Synthesis of G49

[0417] To a solution of 2-fluoroprop-2-enoic acid (23.71 mg, 263.25 umol) in DMF (1.5 mL) were added DIEA (27.22 mg, 210.60 umol, 36.68 uL) and HATU (100.09 mg, 263.25 umol) at 0° C., then G48 (110 mg, 175.50 umol) was added, and it was stirred at 25° C. for 1 hr to give a yellow solution. Then additional 2-fluoroprop-2-enoic acid (23.71 mg, 263.25 umol) and HATU (100.09 mg, 263.25 umol) were added, and it was stirred at 25° C. for another 30 min to give a yellow solution. The mixture was partitioned between EtOAc (10 ml) and water (10 mL). The aqueous phase was extracted with EtOAc (10 mL×2). The combined organic extract was washed with brine (30 mL×5), dried over Na₇SO₄, filtered, concentrated under reduced pressure to give crude product. The crude product was purified by prep-TLC to afford G49 (40 mg, 56.55 umol, 32.22% yield) as a colorless gum.

Procedure for Synthesis of Compound 199

[0418] To a solution of G49 (40 mg, 57.24 umol) in DCM (1 mL) was added TFA (308.00 mg, 2.70 mmol, 0.2 mL) at 0° C. The mixture was stirred at 0° C. for 1 hours to give a yellow mixture. The mixture was concentrated under reduced pressure to give a residue. The residue was dissolved in H₂O (10 mL) and then basified to pH=9 (Na₂CO₃), extracted with EtOAc (20 mL×3). The combined organic layer was dried over anhydrous Na)SO₄, filtered and concentrated under reduced pressure and then lyophilized to afford compound 199 (23.1 mg, 37.97 umol, 66.33% yield, 98.4% purity) as a white powder.

Exceptional Synthetic Route

[0419]
Procedure for Synthesis of H2

[0420] To a mixture of compound H1 (214 mg, 1.75 mmol), DIPEA (1 mL) in MeCN (10 mL) was added compound G10 (500 mg, 1.17 mmol). The reaction solution was stirred at 20° C. for 1 hour to give a yellow mixture. LCMS showed the reaction was completed. The reaction mixture was partitioned with DCM (100 mL) and water (80 mL). The aqueous phase was extracted with DCM (80 mL×2). The combined extract was washed with brine (80 mL×2), dried over anhydrous Na₂SO₄ and filtrated, then concentrated under reduced pressure to give crude product as yellow oil, which was purified by Combi flash to give compound H2 (500 mg) as a yellow gum.

Procedure for Synthesis of H4

[0421] To a mixture of compound H2 (200 mg, 0.822 mmol) in DMF (5 mL) was added HATU (391 mg, 1.03 mmol), TEA (139 mg, 1.37 mmol), and stirred at 20° C. for 30 minutes. Then compound H3 (352 mg, 0.685 mmol) was added to the mixture, and stirred at 60° C. under N₂ atmosphere for 5 hours to give a yellow mixture. LCMS showed the reaction was completed. The mixture cooled to temperature and poured into water (50 mL). The yellow solid precipitated out from the mixture. The mixture was filtrated and the filter cake was washed with water (50 mL) to give a crude product as a yellow powder, which was purified by Combi flash to give compound H4 (302 mg) as a yellow gum.

Procedure for Synthesis of H5

[0422] The compound H4 (300 mg) was followed the same procedure of A7 to obtain 290 mg of compound H5 as a yellow gum.

Procedure for Synthesis of H6

[0423] The compound H5 (200 mg) was followed the same procedure of A6 to obtain 101 mg of compound H6 as a yellow oil.

Procedure for Synthesis of Compound 22

[0424] To a mixture of compound 116 (100 mg, 0.133 mmol) in HBr/HOAc (2 mL, 35%) was stirred at 20° C. for 1 hour to give a yellow mixture. LCMS showed the reaction was completed. To the reaction mixture was added MTBE (10 mL) to precipitate an off-white powder. The white powder was collected by filtration and washed with MTBE (5 mL×2), which was purified by prep-HPLC (0.1% TFA) and then basified by cation exchange resin eluting with 5% NH₃·H₂O/MeOH to give compound 22 (15 mg) as a white powder.

[0425]
Procedure for Synthesis of H8

[0426] To a mixture of compound H2 (207 mg, 0.972 mmol), compound 117 (500 mg, 0.972 mmol) in DCM (8 mL) was added AcOH (58.3 mg, 0.972 mmol). The mixture was stirred at 20° C. for 1 hour and then added NaBH(OAc)₃ (309 mg, 1.46 mmol) to the mixture, and stirred at 20° C. for 24 hours. LCMS show desired MS value. The mixture was partitioned between DCM (50 mL) and saturated NaHCO₃ (50 mL). The DCM phase was washed with NaHCO₃ (50 mL×2), and dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give yellow oil, which was purified by Combi flash to give compound H8 (200 mg) as a yellow oil.

Procedure for Synthesis of H9

[0427] To a mixture of compound H8 (200 mg, 0.281 mmol) in DCM (5 mL) was added TFA (1 mL). The mixture was stirred at 20° C. for 2 hours to give a yellow mixture. LCMS showed the reaction was completed. The mixture was combined and concentrated under reduced pressure to give compound H9 (200 mg) as a yellow oil

Procedure for Synthesis of H10

[0428] To a mixture of compound H9 (200 mg, 0.276 mmol) in THF (5 mL) was added DIPEA (178 mg, 1.38 mmol), compound A5 (152 mg, 0.827 mmol). The yellow mixture was stirred at 25° C. for 1 hour and become black. LCMS showed the reaction was completed. Dimethylamine (2 M, 689 uL) was added to the mixture and stirred at 25° C. for 1 hour to give a brown mixture. LCMS showed desired MS value. The mixture was partitioned between DCM (50 mL) and water (30 mL). The aqueous phase was extracted with DCM (50 mL×2). The combined extracted phase was washed with brine (30 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give brown oil, which was purified by Combi flash to give compound H10 (180 mg) as brown oil.

Procedure for Synthesis of Compound 21

[0429] To a mixture of compound H10 (180 mg, 0.249 mmol) in HBr/HOAc (2.00 mL, 35% purity) was stirred at 20° C. for 1 hour to give a yellow mixture. TLC showed the reaction was completed. To the reaction mixture was added MTBE (10 mL) to precipitate an off-white powder. The white powder was collected by filtration and washed with MTBE (5 mL×2). The crude product was purified by prep-HPLC to give compound 21 (16.2 mg) as a white powder.

[0430]
Procedure for Synthesis of H12

[0431] A mixture of compound H11 (500 mg, 2.06 mmol) and DIPEA (400 mg, 3.09 mmol) in NMP (5 mL) was added (4-methoxyphenyl)methanamine (475 mg, 3.46 mmol). The reaction mixture was stirred at 135° C. for 24 hours under N₂ atmosphere. The mixture was cooled to room temperature, water (50 mL) was added to the reaction mixture and extracted with MTBE (30 mL×3), the combined organic phase was washed with water (20 mL) and brine (20 mL), dried with anhydrous Na₂SO₄ and concentrated under reduced pressure to give the residue. The residue was purified by silica gel column to give compound H12 (910 mg) as a red solid.

Procedure for Synthesis of H13

[0432] To a solution of compound H12 (500 mg, 1.46 mmol) in DMA (5 mL) was added Zn(CN)₂ (103 mg, 0.876 mmol), Pd₂(dba)₃ (134 mg, 0.146 mmol), DPPF (162 mg, 0.292 mmol) and Zn (15.28 mg, 0.234 mmol). The reaction was stirred at 150° C. under microwave condition for 0.5 hour under N₂ atmosphere. LCMS showed the reaction was completed. The mixture was partitioned between with water (30 mL) and EtOAc (30 mL). The aqueous phase was extracted with EtOAc (20 mL). The combined extracts were washed with bine (50 mL), dried over anhydrous Na₂SO₄, filtered and concentrated under reduced pressure to give compound, which was purified by Combi flash to give compound H13 (300 mg) as a red gum.

Procedure for Synthesis of H14

[0433] To a mixture of Raney-Ni (100 mg) in MeOH (30 mL) was added compound H13 (500 mg, 1.73 mmol) and NH₃·H₂O (2.5 mL, 25%). The suspension was degassed under vacuum and purged with H₂ several times, the mixture was stirred at 25° C. under H₂ (15 psi) for 3 hours to give a black mixture. TLC showed the reaction was completed. The mixture was filtered, the filtrate was concentrated under reduced pressure to give compound H14 (400 mg) as a yellow gum.

Procedure for Synthesis of H15

[0434] To a mixture of compound H14 (90.0 mg, 0.307 mmol), DIPEA (165 mg, 1.28 mmol) in MeCN (1 mL) was added compound G10 (110 mg, 256 mmol). The reaction solution was stirred at 25° C. for 1 hour to give a yellow mixture. LCMS showed the reaction was completed. The mixture was partitioned with DCM (30 mL) and water (20 mL). The aqueous phase was extracted with DCM (30 mL×2). The combined extract was washed with brine (30 mL×2), dried over anhydrous Na₂SO₄ and filtrated, then concentrated under reduced pressure to give crude product as yellow oil. The crude product was purified by Combi flash to give compound H15 (100 mg) as a yellow gum.

Procedure for Synthesis of H16

[0435] To a mixture of compound H15 (100 mg, 0.146 mmol) in TFA (1 mL) was stirred at 25° C. for 3 hours, LCMS showed a lot of starting material was still remained, and heated to 60° C. for 12 hours LCMS showed desired MS value, then heated to 80° C. for 14 hours to give a yellow mixture. LCMS showed the reaction was completed. The mixture was partitioned with DCM (50 mL) and saturated solution of NaHCO₃ (30 mL). The aqueous phase was extracted with DCM (50 mL×2). The combined extract was washed with brine (30 mL×2), dried over anhydrous Na₂SO₄ and filtrated, then concentrated under reduced pressure to give compound H16 (100 mg) as a yellow gum.

Procedure for Synthesis of H17

[0436] To a solution of compound H16 (100 mg, crude) and di-tert-butyl dicarbonate (55.6 mg, 0.255 mmol) in DCM (1 mL) was added DIPEA (32.9 mg, 0.255 mmol). The resulting mixture was stirred at 25° C. for 2 hours to give colorless solution. LCMS showed the reaction was completed. The mixture was concentrated under reduced pressure to give compound H17 (102 mg) as a yellow gum.

Procedure for Synthesis of H18

[0437] To a mixture of compound H17 (102 mg) in THF (2 mL) was added DIPEA (248 mg, 1.92 mmol) and compound A5 (106 mg, 0.576 mmol), the mixture was stirred at 25° C. for 1 hour. LCMS showed the reaction was completed. dimethylamine (2M, 383 uL) was added to the mixture. The mixture was stirred at 25° C. for 30 hours to give a brown mixture. LCMS showed the reaction was completed. The mixture was partitioned between DCM (50 mL) and water (30 mL), The aqueous was extracted with DCM (50 mL×2), the combined extracted phase was washed with brine (30 mL), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give a brown oil, which was purified by Combi flash to give compound H18 (80 mg) as a yellow oil.

Procedure for Synthesis of Compound 12

[0438] To a mixture of compound H18 (80 mg, 0.083 mmol) in DCM (2 mL) was added TFA (770 mg, 0.5 mL), the mixture was stirred at 25° C. for 1 hour to give a yellow mixture. LCMS showed the reaction was completed. The mixture was concentrated under reduced pressure to give yellow oil, which was purified by prep-HPLC to give compound 12 (6.4 mg) as a white powder.

[0439]
Procedure for Synthesis of H20

[0440] To a mixture of compound G7 (650 mg, 2.54 mmol) and DIPEA (1.64 g, 12.7 mmol) in NMP (12 mL) was added compound H19 (488 mg, 3.80 mmol). The reaction mixture was stirred at 140° C. for 28 hours under N₂ atmosphere to give a brown solution. LCMS showed the reaction was completed. The reaction was conducted two pots in parallel. The reaction mixture was combined and concentrated under reduced pressure to give crude product as a brown gum, which was washed with MeOH (15 mL) to give compound H20 (1.09 g) as a yellow powder.

Procedure for Synthesis of H21

[0441] To a mixture of compound H20 (400 mg, 1.31 mmol) in POCl₃ (5 mL) was added N, N-diethylaniline (588 mg, 3.94 mmol). The mixture was stirred at 90° C. for 1 hour to give a yellow mixture. The mixture was concentrated under reduced pressure to give compound H21 (420 mg) as a brown oil.

Procedure for Synthesis of Compound 14

[0442] To a mixture of compound H21 (300 mg, 0.929 mmol), DIPEA (2.40 g, 18.6 mmol) in CH₃CN (5 mL) was added compound A16 (533 mg, 1.39 mmol). The reaction solution was stirred at 25° C. for 1 hour to give a yellow mixture. LCMS showed the reaction was completed. The mixture was portioned between DCM (80 mL) and water (50 mL), the aqueous phase was extracted by DCM (80 mL×2), the combined extracted phase was washed with brine (80 mL×2), dried over anhydrous Na₂SO₄, filtered, concentrated under reduced pressure to give a yellow oil. Crude product was purified by Combi flash and then by prep-TLC. The product was lyophilized to give compound 14 (45.5 mg) as a yellow powder.

[0443]
Procedure for Synthesis of H23

[0444] To a solution of compound G26 (500 mg, 966.07 umol) and compound H22 (271 mg, 1.93 mmol) in DMF (10 mL) was added Cs₂CO₃ (630 mg, 1.93 mmol). The resulting mixture was heated at 30-40° C. and stirred for 16 hr to give yellow solution. LCMS showed the reaction was completed. The mixture was filtered and was partitioned between EtOAc (50 mL). The aqueous layer was extracted with EtOAc (50 mL*3). The organic layer was washed with saturated brine (50 mL), dried over anhydrous Na₂SO₄, filtered, and concentrated under reduced pressure to give the crude product as a yellow oil. The crude product was purified by combi flash to give compound H23 (490 mg) as a yellow oil.

Procedure for Synthesis of H24

[0445] The compound H23 (490 mg) was followed the same procedure of B7 to obtain 440 mg of compound H24 as a yellow powder.

Procedure for Synthesis of H25

[0446] The compound H24 (390 mg) was followed the same procedure of E3 to obtain 310 mg of compound H25 as a yellow powder.

Procedure for Synthesis of Compound 41

[0447] The compound H25 (150 mg) was followed the same procedure of compound 44 to obtain 23 mg of compound 41 as a yellow powder.

[0448]
Procedure for Synthesis of H28

[0449] To a solution of compound H26 (500 mg, 2.27 mmol), compound H27 (638 mg, 3.41 mmol) and PPh₃ (893 mg, 3.41 mmol) in THF (10 mL) was added DIAD (689 mg, 3.41 mmol, 662 u) at 0° C. The resulting mixture was stirred at 15° C. for 24 hr to give yellow solution. TLC showed most of the starting material consumed. The reaction mixture was quenched by addition H₂O (30 mL) and extracted with EtOAc (30 mL×2). The combined organic layers were washed with brine (10 mL×2), dried over Na₂SO₄, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to give compound H28 (570 mg) as yellow oil.

Procedure for Synthesis of H29

[0450] To a mixture of compound G26 (1 g, 1.93 mmol) in dioxane (10 mL) and H₂O (10 mL) was added NaOH (309 mg, 7.73 mmol) and the mixture was stirred at 50° C. for 12 hours to give a yellow mixture. LCMS showed the desired product was observed. The mixture was concentrated under reduced pressure and adjusted to pH=3-4 and the mixture was filtered, and collected the white solid to afford compound H29 (620 mg) as a yellow solid.

Procedure for Synthesis of H30

[0451] To a mixture of compound H29 (500 mg, 1.10 mmol) in toluene (10 mL) were added POBr₃ (944 mg, 3.29 mmol, 334 uL) and N,N-diethylaniline (16.3 mg, 109 umol, 17.56 uL) at 15° C., the mixture was stirred at 100° C. for 3 hours to give a yellow mixture. LCMS showed the desired product was observed. The mixture was concentrated under pressure to give the crude product. The crude product was triturated with (PE/EA=3/1) at 15° C. for 30 min to afford compound H30 (330 mg) as a black brown solid.

Procedure for Synthesis of H31

[0452] To a mixture of compound H30 (330 mg, 636 umol) and compound H28 (247 mg, 636 umol) in dioxane (5 mL) and H₂O (2 mL) were added Na₂CO₃ (134 mg, 1.27 mmol, 2 eq) and Pd(dppf)Cl₂ (46.58 mg, 63.66 umol) and the mixture was stirred at 80° C. for 16 hours under N₂ to give a black mixture. LCMS showed the desired product was observed. The mixture was partitioned between EtOAc (15 ml) and water (10 mL). The aqueous phase was extracted with EtOAc (10 mL×2). The combined organic extract was washed with brine (10 mL), dried over Na₂SO₄, filtered, concentrated under reduced pressure to give crude product. The crude product was purified by combi flash (PE/EA=1/1) to afford compound H31 (50 mg) as a red solid.

Procedure for Synthesis of H32

[0453] The compound H31 (50 mg) was followed the same procedure of compound B7 to obtain 43 mg of compound H32 as a yellow powder.

Procedure for Synthesis of H33

[0454] The compound H32 (11.5 mg) was followed the same procedure of compound G31 to obtain 10 mg of compound H33 as a yellow powder.

Procedure for Synthesis of Compound 87

[0455] The compound H33 (10 mg) was followed the same procedure of compound A7 to obtain 3 mg of compound 87 as a yellow powder.

[0456]
Procedure for Synthesis of H34

[0457] The compound G26 (100 mg) was followed the same procedure of compound B7 to obtain 80 mg of compound H34 as a yellow powder.

Procedure for Synthesis of H35

[0458] To a solution of H34 (I g, 2.05 mmol, 1 eq), pyridine (973.39 mg, 12.31 mmol, 993.25 uL, 6 eq) in THF (10 mL) and NMP (2 mL) was added CbzCl (1.40 g, 8.20 mmol, 1.17 mL, 4 eq) at 20° C. The reaction was stirred at 20° C. for 12 h to give pale brown solution. Additional pyridine (0.5 mL) and CbzCl (0.6 mL) were added and the reaction was heated at 50° C. for further 5 h to give pale brown solution. The reaction was cooled to rt., diluted with EA (100 mL), washed with water (80 mL*2) and brine (80 mL). The organic layer was dried over Na₂SO₄, concentrated in vacuum to give pale brown oil. The oil was purified by flash column to give H35 (650 mg, 1.05 mmol, 50.98% yield) as off-white solid.

Procedure for Synthesis of H36

[0459] To a solution of H35 (600 mg, 965.08 umol, 1 eq) in THF (12 mL) was added MeMgBr (3 M, 643.39 uL, 2 eq) at 0° C. The reaction was allowed to warm to 0° C. and stirred for further 1 h to give pale yellow solution. Monitor LCMS showed no reaction. Additional 2 eq of MeMgBr was added and the reaction was stirred at 20° C. for further 4 h. TLC showed two major spot. The reaction as diluted quenched with water (40 mL), extracted with EA (40 mL). The organic layer was washed with brine (30 mL), dried over Na₂SO₄, concentrated in vacuum to give crude pale yellow oil. The crude oil was purified by flash column to give H36 (200 mg, 358.65 umol, 37.16% yield) as pale yellow gum.

Procedure for Synthesis of H37

[0460] The compound H36 (200 mg) was followed the same procedure of compound B7 to obtain 140 mg of compound H37 as a yellow gum.

Procedure for Synthesis of Compound 167

[0461] The compound H37 (100 mg) was followed the same procedure of compound 44 to obtain 74 mg of compound 167 as a white solid.

• [0462] D. B. Bregman, R. G. Pestell and V. J. Kidd. Cell cycle regulation and RNA polymerase II. Front Biosci. 2000 February; 1(5): D244-57.
• [0463] D. Desai, H. C. Wessling, R. P. Fisher, and D. O. Morgan. Effects of phosphorylation by CAK on cyclin binding by CDCl2 and CDK2. Mol. Cell Biol. 1995 January; 15(1): 345-350.
• [0464] S. Akhtar, M. Heidemann, J. R. Tietjen, D. W. Zhang, R. D. Chapman, D. Eick, and A. Z. Ansari. TFIIH Kinase Places Bivalent Marks on the Carboxy-Terminal Domain of RNA Polymerase II. Mol. Cell. 2009 May; 15; 34(3):387-93.
• [0465] S. Larochelle, R. Amat, K. G. Cutter, M. Sank), C. Zhang, J. J. Allen, K. M. Shokat, D. L. Bentley and R. P. Fisher. Cyclin-dependent kinase control of the initiation-to-elongation switch of RNA polymerase H. Nat. Struct. Mol. Biol. 2012 November; 19(11):1108-15.
• [0466] G. I. Shapiro. Cyclin-Dependent Kinase Pathways as Targets for Cancer Treatment. J. Clin. Oncol. 2006 April; 10; 24(11):1770-83.
• [0467] G. Lolli and L. N. Johnson. CAK-Cyclin-dependent Activating Kinase: a key kinase in cell cycle control and a target for drugs? Cell Cycle. 2005 April; 4(4):572-7.
• [0468] T. I. Lee and R. A. Young. Transcriptional Regulation and its misregulation in Disease. Cell. 2013 March; 14; 152(6):1237-51.
• [0469] S. Nekhai, M. Zhou, A. Fernandez, W. S. Lane, Ned J. C. Lamb, J. Brady, A. Kumar. Biochem. J. 2002 June; 15; 364 (Pt 3):649-57.
• [0470] Y. K. Kim, C. F. Bourgeois, R. Pearson, M. Tyagi, M. J. West, J. Wong, S. Y. Wu, C. M. Chiang, and J. Karn. Recruitment of TFIIH to the HIV LTR is a rate-limiting step in the emergence of HIV from latency. EMBO. J. 2006 August; 9; 25(15): 3596-3604.
• [0471] A. J. Kapasi and D. H. Spector. Inhibition of the Cyclin-Dependent Kinases at the Beginning of Human Cytomegalovirus Infection Specifically Alters the Levels and Localization of the RNA Polymerase II Carboxyl-Terminal Domain Kinases cdk9 and cdk7 at the Viral Transcriptosome. J. Virol. 2008 January; 82(1): 394-407.
• [0472] Eickhoff et al, Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhibitors. PCT WO2013/128028A1

[0473]

TABLE 1
Enzymatic activity of CDKs (1, 2, 5 and 7) and selectivity of CDK7
# cpds	CDK1	CDK2	CDK5	CDK7	CDK1/CDK7*	CDK2/CDK7**	CDK5/CDK7***
1	C	B	B	A	B	B	C
2	B	B	B	A	B	B	C
3	B	B	A	A	C	C	C
5	C	B	B	A	B	B	C
6	C	C	B	A	A	A	C
7	C	C	C	A	A	A	B
8	C	C	B	A	A	B	B
10	C	B	B	A	B	B	C
11	C	C	C	A	A	A	A
12	C	C	B	A	A	B	C
14	C	C	B	A	A	B	B
15	C	B	B	A	A	B	B
16	C	B	B	A	B	B	C
18	C	B	B	A	A	B	B
19	B	A	A	A	C	C	C
20	C	C	B	A	B	A	B
21	C	C	B	A	A	B	B
22	C	B	B	A	A	B	C
23	C	C	B	A	B	C	C
24	B	B	B	A	B	C	C
25	B	B	A	A	B	C	C
26	C	C	C	A	A	A	A
27	C	C	C	A	B	B	B
28	C	C	C	B	B	B	B
29	C	C	C	B	B	B	B
30	C	C	C	B	B	B	B
31	C	C	C	A	A	A	A
32	C	C	C	A	A	A	A
33	C	C	C	B	B	B	B
34	C	C	C	A	A	A	A
35	C	C	C	A	B	B	B
36	C	C	C	A	A	A	A
37	C	C	C	B	B	B	B
38	C	C	C	B	B	B	B
39	C	C	C	A	A	A	B
40	C	C	C	A	A	A	B
41	C	C	C	A	B	B	B
42	C	C	C	B	B	B	B
43	C	C	C	B	B	B	B
44	C	C	C	A	A	A	A
45	C	C	C	A	A	A	A
46	C	C	C	A	A	A	A
47	C	C	C	A	A	A	B
48	C	C	C	A	A	A	A
49	C	C	C	A	A	A	A
50	C	C	C	A	A	A	A
51	C	C	C	A	A	A	A
52	C	C	C	A	A	A	A
53	C	C	C	A	A	A	A
54	C	C	C	A	A	A	A
55	C	C	C	A	A	A	B
56	C	C	C	A	A	A	A
57	C	C	C	A	A	A	A
58	C	C	C	A	A	A	A
59	C	C	C	A	A	A	A
60	C	C	C	A	A	A	A
61	C	C	C	A	A	A	A
62	C	C	C	A	A	A	A
63	C	C	C	A	A	A	A
64	C	C	C	A	A	A	A
65	C	C	C	A	A	A	A
66	C	C	C	A	A	A	A
67	C	C	C	A	A	A	A
68	C	C	C	A	A	A	A
69	C	C	C	A	B	B	B
70	C	C	C	A	A	A	A
71	C	C	C	A	B	B	B
72	C	C	C	A	A	A	A
73	C	C	C	A	A	A	B
74	C	C	B	A	B	B	B
75	C	C	C	B	B	B	B
76	C	C	C	A	A	A	A
77	C	C	C	A	A	A	A
78	C	C	C	A	A	A	B
79	C	C	C	A	A	A	A
80	C	C	C	A	A	A	A
81	C	C	C	B	B	B	B
82	C	C	C	A	A	A	A
83	C	C	C	A	A	A	A
84	C	C	C	B	B	B	B
85	C	C	C	B	B	B	B
86	C	C	C	C	C	C	C
87	C	C	C	A	A	A	A
88	C	C	C	B	B	B	B
89	C	C	C	C	C	C	C
90	C	C	C	B	B	B	B
91	C	C	C	B	B	B	B
92	C	C	C	B	B	B	B
93	C	C	C	C	C	C	C
94	C	C	C	A	A	A	A
95	C	C	C	A	A	A	A
96	C	C	C	B	B	B	B
97	C	C	C	B	B	B	B
98	C	C	C	B	B	B	B
99	C	C	C	B	B	B	B
100	C	C	C	C	C	C	C
101	C	C	C	B	B	B	B
102	C	C	C	B	B	B	B
103	C	C	C	A	B	B	B
104	C	C	C	B	B	B	B
105	C	C	C	B	B	B	B
106	C	C	C	B	C	C	C
107	C	C	C	B	B	B	B
108	C	C	C	B	C	C	C
109	C	C	C	A	A	A	A
110	C	C	C	A	B	B	B
111	C	C	C	A	A	A	A
112	C	C	C	B	B	B	B
113	C	C	C	A	B	B	B
114	C	C	C	A	A	A	A
115	C	C	C	B	B	B	B
116	C	C	C	A	A	A	A
117	C	C	C	B	B	B	B
118	C	C	C	A	A	A	A
119	C	C	C	B	B	B	B
120	C	C	C	A	A	A	A
121	C	C	C	A	B	B	B
122	C	C	C	A	A	A	A
123	C	C	C	A	A	A	A
124	C	C	C	A	B	B	B
125	C	C	C	B	B	B	B
126	C	C	C	B	B	B	B
127	C	C	C	B	B	B	B
128	C	C	C	A	A	A	A
129	C	C	C	B	B	B	B
130	C	C	C	A	A	A	A
131	C	C	C	A	A	A	A
132	C	C	C	A	A	A	A
133	C	C	C	A	A	A	A
134	C	C	C	A	A	A	A
135	C	C	C	B	B	B	B
136	C	C	C	B	B	B	B
137	C	C	C	A	A	A	A
138	C	C	C	A	A	A	A
139	C	C	C	A	A	A	A
140	C	C	C	B	B	B	B
141	C	C	C	A	A	A	A
142	C	C	C	A	A	A	A
143	C	C	C	B	B	B	B
144	C	C	C	A	B	B	B
145	C	C	C	A	A	A	A
146	C	C	C	A	A	A	A
147	C	C	C	A	A	A	A
148	C	C	C	A	B	B	B
149	C	C	C	A	B	C	B
150	C	C	C	A	A	A	A
151	C	C	C	A	A	A	A
152	C	C	C	A	A	A	A
153	C	C	C	A	A	A	A
154	C	C	C	A	A	A	A
155	C	C	C	A	A	A	A
156	C	C	C	B	B	B	B
157	C	C	C	A	B	B	B
158	C	C	C	A	A	A	A
159	C	C	C	B	B	B	B
160	C	C	C	A	A	A	A
161	C	C	C	A	A	A	A
162	C	C	C	A	A	A	A
163	C	C	C	A	A	A	A
164	C	C	C	A	A	A	A
165	C	C	C	B	B	B	B
166	C	C	C	A	A	A	A
167	C	C	C	B	B	B	B
168	C	C	C	A	B	B	B
169	C	C	C	A	B	B	B
170	C	C	C	B	B	B	B
171	C	C	C	A	A	A	A
172	C	C	C	A	A	A	A
173	C	C	C	A	A	A	A
174	C	C	C	A	A	A	A
175	C	C	C	A	A	A	A
176	C	C	C	A	A	A	A
177	C	C	C	A	A	A	A
178	C	C	C	A	A	A	A
179	C	C	C	A	A	A	A
180	C	C	C	A	A	A	A
181	C	C	C	A	A	A	A
182	C	C	C	B	B	B	B
183	C	C	C	B	B	B	B
184	C	C	C	A	A	A	A
185	C	C	C	A	A	A	A
186	C	C	C	A	A	A	A
187	C	C	C	A	A	A	A
188	C	C	C	A	A	A	A
189	C	C	C	B	B	B	B
190	C	C	C	A	A	A	A
191	C	C	C	A	A	A	A
192	C	C	C	A	A	A	A
193	C	C	C	A	A	A	A
194	C	C	C	A	A	A	A
195	C	C	C	A	A	A	A
196	C	C	C	C	C	C	C
197	C	C	C	A	A	A	A
198	C	C	C	A	B	B	B
199	C	C	C	A	A	A	A
200	C	C	C	A	B	B	B
201	C	C	C	A	B	B	B
202	C	C	C	A	B	B	B
203	C	C	C	A	A	A	A
204	C	C	C	A	A	A	A
205	C	C	C	A	B	B	B
206	C	C	C	A	A	A	A
207	C	C	C	B	B	B	B
208	C	C	C	B	B	B	B
209	C	C	C	A	A	A	A
210	C	C	C	A	B	B	B
211	C	C	C	A	A	A	A
212	C	C	C	A	A	A	A
213	C	C	C	C	C	C	C
214	C	C	C	A	A	A	A
215	C	C	C	A	A	A	A
216	C	C	C	B	B	B	B
Activity range: A indicates IC50 ≤ 100 nM, B indicates 100 ≤ IC50 ≤ 1,000 nM, C indicates IC50 > 1,000 nM
*CDK1/CDK7: Selectivity of CDK7 inhibition over CDK1 inhibition [fold]
**CDK2/CDK7: Selectivity of CDK7 inhibition over CDK2 inhibition [fold]
***CDK5/CDK7: Selectivity of CDK7 inhibition over CDK5 inhibition [fold]
Selectivity range: A indicates [fold] > 500, B indicates 50 < [fold] ≤ 500, C indicates [fold] ≤ 50

[0474]

TABLE 2
H460 viability assay
	# cpds	IC50
	1	B
	2	A
	3	A
	5	A
	6	A
	7	A
	8	A
	9	B
	10	A
	11	A
	12	A
	13	A
	14	A
	15	A
	16	A
	18	A
	19	B
	20	A
	21	B
	22	B
	23	B
	24	B
	25	A
	26	A
	27	A
	Activity range: A indicates IC50 ≤ 1 uM, B indicates 1 < IC50 ≤ 10 uM, C indicates IC50 > 10 uM

[0475]

TABLE 3
MV4-11 viability assay
	# cpds	IC50
	3	A
	11	A
	20	A
	25	A
	26	A
	27	A
	28	A
	29	A
	30	A
	31	A
	32	A
	33	A
	34	A
	35	A
	36	A
	37	A
	38	A
	39	A
	40	A
	41	A
	42	A
	43	A
	44	A
	45	A
	46	A
	47	A
	48	A
	49	A
	50	A
	51	A
	52	A
	53	A
	54	A
	55	A
	56	A
	57	A
	58	A
	59	A
	60	A
	61	A
	62	A
	63	A
	64	A
	65	A
	66	A
	67	A
	68	A
	69	A
	70	B
	71	A
	72	A
	73	A
	74	A
	75	A
	76	A
	77	A
	78	A
	79	A
	Activity range: A indicates IC50 ≤ 1 uM, B indicates 1 < IC50 ≤ 10 uM, C indicates IC50 > 10 uM

[0476]

TABLE 4
A2780 viability assay
	# cpds	IC50
	3	A
	11	A
	20	A
	25	A
	26	A
	27	A
	28	A
	29	A
	30	A
	31	A
	32	A
	33	A
	34	A
	35	A
	36	A
	37	A
	38	A
	39	A
	40	A
	41	A
	42	A
	43	A
	44	A
	45	A
	46	A
	47	A
	48	A
	49	A
	50	A
	51	A
	52	A
	51	A
	52	A
	53	A
	54	A
	55	A
	56	A
	57	A
	58	B
	59	A
	60	A
	61	A
	62	A
	63	B
	64	A
	65	A
	66	A
	67	A
	68	A
	69	A
	70	B
	71	A
	72	A
	73	B
	74	A
	75	A
	76	A
	77	B
	78	A
	79	A
	80	A
	81	A
	82	A
	83	A
	84	A
	85	A
	86	B
	87	A
	88	A
	89	B
	90	A
	91	A
	92	A
	93	A
	94	A
	95	A
	96	A
	97	A
	98	A
	99	A
	100	B
	101	A
	102	A
	103	A
	104	A
	105	A
	106	A
	107	A
	108	A
	109	B
	110	A
	111	A
	112	A
	113	A
	114	B
	115	A
	116	A
	117	A
	118	A
	119	A
	120	A
	121	A
	122	A
	123	A
	124	A
	125	A
	126	A
	127	A
	128	A
	130	A
	133	A
	137	A
	147	A
	150	A
	151	A
	153	A
	154	A
	156	A
	157	A
	158	A
	159	A
	160	A
	161	A
	162	A
	163	A
	164	A
	165	A
	166	A
	167	A
	168	A
	169	A
	170	A
	171	A
	172	A
	173	A
	174	A
	175	A
	176	A
	177	A
	178	A
	179	A
	180	A
	181	A
	182	A
	183	A
	184	A
	185	A
	186	A
	187	A
	188	A
	189	B
	190	A
	191	A
	192	A
	193	A
	194	A
	195	A
	196	B
	197	A
	198	A
	199	A
	200	A
	201	A
	202	A
	203	A
	204	A
	205	A
	206	A
	207	A
	208	B
	209	A
	210	A
	211	A
	212	A
	213	B
	214	A
	215	A
	Activity range: A indicates IC50 ≤ 1 uM, B indicates 1 < IC50 ≤ 10 uM, C indicates IC50 > 10 uM

[0477]

TABLE 5
OVCAR-3 viability assay
	# cpds	IC50
	3	A
	11	A
	20	A
	25	A
	26	A
	27	A
	28	A
	29	A
	30	A
	31	A
	32	A
	33	A
	34	A
	35	A
	36	A
	37	A
	38	A
	39	A
	40	A
	41	A
	42	A
	43	A
	44	A
	45	A
	46	A
	47	A
	48	A
	49	A
	50	A
	51	A
	52	A
	53	A
	54	A
	55	A
	56	A
	57	A
	58	B
	59	A
	60	A
	61	A
	62	A
	63	B
	64	A
	65	A
	66	A
	67	A
	68	A
	69	A
	70	B
	71	A
	72	A
	73	B
	74	A
	75	A
	76	A
	77	B
	78	B
	79	A
	80	A
	81	A
	82	A
	83	A
	84	A
	85	A
	86	A
	87	A
	88	A
	89	B
	90	A
	91	A
	92	A
	93	B
	94	A
	95	A
	96	A
	97	A
	98	A
	99	A
	100	B
	101	A
	102	A
	103	A
	104	A
	105	A
	106	A
	107	A
	108	A
	109	B
	110	A
	111	A
	112	A
	113	A
	114	A
	115	B
	116	A
	117	A
	118	A
	119	A
	120	A
	121	A
	122	A
	123	A
	124	A
	125	A
	126	A
	127	A
	128	A
	118	A
	119	A
	120	A
	121	A
	122	A
	123	A
	124	A
	125	A
	126	A
	127	A
	128	A
	130	B
	126	A
	127	A
	133	A
	137	A
	147	A
	150	A
	151	A
	153	A
	154	B
	156	B
	157	B
	158	A
	159	B
	160	A
	161	A
	162	B
	163	A
	164	A
	165	A
	166	C
	167	A
	168	A
	169	A
	170	B
	171	A
	172	A
	173	A
	174	A
	175	A
	176	A
	177	A
	178	A
	179	A
	180	A
	181	A
	182	B
	Activity range: A indicates IC50 ≤ 1 uM, B indicates 1 < IC50 ≤ 10 uM, C indicates IC50 > 10 uM

[0478]

TABLE 6
CDK7 selectivity profile in CDKs family
	CDKs family	Compound 11 (uM)
	CDK1/CycA2	>10
	CDK1/CycB1	>10
	CDK1/CycE1	>10
	CDK2/CycA2	>10
	CDK2/CycD1	>10
	CDK2/CycE1	>10
	CDK3/CycC	>10
	CDK3/CycE1	>10
	CDK4/CycD1	>10
	CDK4/CycD2	>10
	CDK4/CycD3	>10
	CDK5/p25NCK	>10
	CDK5/p35NCK	7.86
	CDK6/CycD1	>10
	CDK6/CycD2	>10
	CDK6/CycD3	>10
	CDK7/CycH/MAT1	0.025
	CDK8/CycC	>10
	CDK9/CycK	>10
	CDK9/CycT1	>10
	CDK12wt/CycK	>10
	CDK13/CycK	>10
	CDK16/CycY	>10
	CDK17/p35NCK	>10
	CDK18/CycY	>10
	CDK19/CycC	>10
	CDK20/CycH	>10
	CDK20/CycT1	>10

[0479]

TABLE 7
Summarized compounds 1-216 in terms of their structures and corresponding characteristics
#cpds	Structure	Characterization Data
1		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 10.28 (1H, brs), 10.25 (1H, brs), 8.86 (1H, brs), 8.13 (1H, s), 7.88 (1H, d, J = 8.0 Hz), 7.80 (1H, s), 7.72 (1H, s), 7.65 (1H, d, J = 7.6 Hz), 7.60 (1H, d, J = 7.6 Hz), 7.44 (1H, t, J = 8.0 Hz), 7.28 (1H, t, J = 7.6 Hz), 7.12 (1H, d, J = 7.2 Hz), 6.75 (1H, td, J = 15.6, 6.0 Hz,), 6.28 (1H, d, J = 15.6 Hz), 4.59 (2H, s), 4.42-4.54 (2H, m), 3.06 (2H, d, J = 5.2 Hz), 2.85- 2.98 (3H, m), 2.65-2.75 (1H, m), 2.18 (6H, s), 1.64-1.76 (2H, m), 1.23 (6H, d, J = 7.2 Hz), 1.03-1.15 (2H, m); LCMS: 95.8%, MS (ESI): m/z 611.3 [M + H]+
2		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 10.12 (1H, brs), 8.85 (1H, brs), 7.70 (1H, s), 7.36-7.42 (2H, m), 7.24-7.36 (2H, m), 7.17 (1H, d, J = 7.6 Hz), 7.07 (1H, s), 6.90 (1H, dd, J = 8.0, 1.6 Hz), 6.63-6.74 (2H, m), 6.21 (1H, d, J = 15.2 Hz), 4.55 (2H, s), 4.39-4.50 (2H, m), 2.99-3.08 (2H, m), 2.81-2.97 (3H, m), 2.66-2.77 (1H, m), 2.16 (6H, s), 1.61-1.76 (2H, m), 1.22 (6H, d, J = 7.2 Hz), 0.99-1.13 (2H, m); LCMS: 100%, MS (ESI): m/z 584.2 [M + H]+.
3		White powder; 1H-NMR (DMSO-d6, 400 MHz): δ 8.65 (1H, brs), 7.89 (1H, brs), 7.62 (1H, s), 7.48-7.59 (3H, m), 7.31-7.43 (2H, m), 7.16-7.22 (1H, m), 7.09-7.15 (1H, m), 6.95-7.06 (1H, m), 6.61 (1H, t, J = 5.6 Hz), 6.56 (1H, s), 6.21 (1H, d, J = 15.2 Hz), 4.83 (2H, d, J = 5.2Hz), 4.55- 4.65 (2H, m), 3.10-3.20 (2H, m), 2.98-3.08 (1H, m), 2.80- 2.89 (3H, m), 2.30 (6H, s), 1.77-1.79 (2H, m), 1.28-1.32 (8H, m); LCMS: 100%, MS (ESI): m/z 629.4 [M + Na]+
4		white powder; 1H-NMR (CDCl3, 400 MHz): δ 7.56 (1H, s), 7.42-7.48 (2H, m), 7.26-7.32 (1H, m), 7.17-7.24 (1H, m), 7.14 (1H, brs), 7.07-7.12 (1H, m), 6.88-6.98 (2H, m), 6.60- 6.70 (2H, m), 6.07 (1H, d, J = 15.2 Hz), 4.77 (2H, d, J = 6.0 Hz), 4.68-4.76 (2H, m), 3.09 (2H, d, J = 5.6 Hz), 2.96- 3.04 (1H, m), 2.86-2.96 (3H, m), 2.26 (6H, s), 1.76-1.90 (2H, m), 1.23-1.34 (8H, m); LCMS: 100%, MS (ESI): m/z 584.4 [M + H]+.
5		white powder; 1H-NMR (CDCl3, 400 MHz): δ 7.79 (1H, brs), 7.60 (1H, s), 7.40-7.50 (1H, m), 7.26-7.33 (2H, m), 7.19 (1H, s), 7.05-7.12 (2H, m), 6.93 (1H, d, J = 7.6 Hz), 6.75 (1H, d, J = 7.6 Hz), 6.71 (1H, brs), 6.41 (1H, d, J = 16.4 Hz), 6.24-6.34 (1H, m), 5.74 (1H, d, J = 10.0 Hz), 4.62-4.75 (4H, m), 2.96-3.06 (1H, m), 2.83-2.95 (3H, m), 1.80-1.84 (2H, m), 1.21-1.33 (8H, m); LCMS: 100%, MS (ESI): m/z 527.3 [M + H]+.
6		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 7.56 (1H, s), 7.33 (1H, d, J = 8.0 Hz), 7.24-7.28 (1H, m), 6.92 (1H, d, J = 6.8 Hz), 6.80-6.88 (2H, m), 6.63 (1H, t, J = 4.8 Hz), 6.53 (1H, d, J = 16.0 Hz), 4.76-4.83 (2H, m), 4.63-4.70 (2H, m), 3.65-3.80 (3H, m), 3.53-3.56 (1H, m), 3.21-3.25 (2H, m), 3.09-3.14 (1H, m), 2.91-3.03 (3H, m), 2.35 (6H, s), 1.94-1.97 (2H, m), 1.86-1.90 (4H, m), 1.45-1.48 (2H, m), 1.27 (6H, d, J = 7.2 Hz); LCMS: 100%, MS (ESI): m/z 576.3 [M + H]+.
7		white powder; 1H-NMR (CDCl3, 400 MHz): δ 7.49 (1H, s), 7.38-7.40 (2H, m), 7.14-7.22 (3H, m), 7.04-7.06 (2H, m), 6.87 (1H, d, J = 8.0 Hz), 6.58-6.59 (1H, m), 6.53 (1H, t, J = 4.8 Hz), 6.33-6.37 (1H, d, J = 16.8 Hz), 6.12-6.14 (1H, m), 5.69 (1H, d, J = 10.8 Hz), 4.64-4.71 (4H, m), 2.82-2.95 (4H, m), 1.79-1.82 (2H, m), 1.19-1.27 (8H, m); LCMS: 91.6%, MS (ESI): m/z 527.3 [M + H]+.
8		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 10.26- 10.27 (1H, s), 10.12-10.14 (1H, s), 8.85-8.69 (1H, brs), 8.21 (1H, s), 7.92 (1H, d, J = 8.0 Hz), 7.72 (1H, s), 7.65-7.68 (1H, m), 7.37-7.49 (3H, m), 7.27-7.31 (1H, m), 7.19-7.23 (1H, m), 6.73-6.76 (1H, m), 6.28 (1H, d, J = 15.6 Hz), 4.63 (2H, s), 4.42-4.47 (2H, m), 3.06 (2H, d, J = 5.2 Hz), 2.82- 2.94 (3H, m), 2.70-2.77 (1H, m), 2.17 (6H, s), 1.64-1.69 (2H, m), 1.22 (6H, d, J = 7.2 Hz), 1.02-1.11 (2H, m); LCMS: 100.0%, MS (ESI): m/z 611.3 [M + H]+.
9		white powder; 1H-NMR (CDCl3, 400 MHz): δ 8.47-8.49 (2H, s), 7.97-7.99 (1H, m), 7.61-7.63 (1H, m), 7.55-7.58 (1H, m), 7.52 (1H, s), 7.38-7.49 (4H, m), 7.22-7.25 (1H, m), 7.04-7.11 (1H, m), 6.63-6.65 (1H, m), 6.35-6.40 (1H, m), 4.72-4.77 (1H, m), 4.78-4.55 (2H, m), 4.26-4.30 (1H, m), 3.19-3.21 (2H, m), 2.92-3.02 (2H, m), 2.76-2.83 (2H, m), 2.35 (6H, s), 1.79-7.82 (2H, m), 1.14-1.29 (8H, m); LCMS: 95.3%, MS (ESI): m/z 619.4 [M + H]+.
10		white powder; 1H-NMR (CDCl3, 400 MHz): δ 7.60 (1H, s), 7.44-7.53 (4H, m), 7.22-7.26 (1H, m), 7.08 (1H, t, J = 7.6 Hz), 6.93-7.00 (3H, m), 6.86 (1H, d, J = 7.6 Hz), 6.71 (1H, t, J = 6.2 Hz), 6.13 (1H, d, J = 15.6 Hz), 4.79 (2H, d, J = 6.4 Hz), 4.71-4.75 (2H, m), 3.12-3.15 (2H, m), 2.99-3.06 (1H, m), 2.89-2.96 (3H, m), 2.30 (6H, s), 1.86-1.89 (2H, m), 1.24-1.33 (8H, m); LCMS: 100.0%, MS (ESI): m/z 584.4 [M + H]+.
11		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 10.51 (1H, brs), 8.44-8.50 (3H, m), 7.75 (1H, d, J = 5.6 Hz), 7.64 (1H, s), 7.55-7.60 (1H, m), 7.46-7.53 (3H, m), 7.42 (1H, t, J = 8.0 Hz), 7.33 (1H, d, J = 7.2 Hz), 6.78-6.85 (1H, m), 6.36 (1H, d, J = 15.2 Hz), 4.25-4.43 (4H, m), 3.08 (2H, d, J = 5.2 Hz), 2.72-2.86 (4H, m), 2.19 (6H, s), 1.60-1.70 (2H, m), 1.19 (6H, d, J = 7.2 Hz), 1.05-1.10 (2H, m); LCMS: 98.9%, MS (ESI): m/z 619.4 [M + H]+.
12		white powder; 1H-NMR (CDCl3, 400 MHz): δ 9.36 (1H, brs), 8.51 (1H, d, J = 9.2 Hz), 8.14-8.17 (2H, m), 7.70 (1H, d, J = 6.8 Hz), 7.66 (1H, d, J = 6.8 Hz), 7.60 (1H, s), 7.34- 7.38 (1H, m), 7.02-7.11 (1H, m), 6.32 (1H, d, J = 16.0 Hz), 5.16 (2H, d, J = 6.0 Hz), 4.78-4.84 (2H, m), 3.18 (2H, d, J = 6.4 Hz), 2.94-3.03 (4H, m), 2.33 (6H, s), 1.92-1.97 (2H, m), 1.30-1.45 (2H, m), 1.25 (6H, d, J = 6.8 Hz); LCMS: 95.9%, MS (ESI): m/z 565.3 [M + Na]+.
13		white powder; 1HNMR (DMSO-d6, 400 MHz): δ 9.93 (1H, brs), 8.89 (1H, brs), 7.81-7.83 (1H, m), 7.72 (1H, s), 7.23- 7.31 (2H, m), 7.15 (1H, d, J = 8.0 Hz), 7.06 (1H, s), 6.86 (1H, dd, J = 7.6, 2.0 Hz), 6.69-6.75 (2H, m), 6.46 (1H, d, J = 15.6) 4.50-4.55 (4H, m), 3.03 (2H, d, J = 4.8 Hz) 2.84- 2.93 (4H, m), 2.16 (6H, s), 1.75-1.80 (2H, m), 1.18-1.23 (8H, m); LCMS: 100%, MS (ESI): m/z 624.3 [M + Na]+.
14		yellow powder; 1H-NMR (CDCl3, 400 MHz): δ 7.74 (1H, brs), 7.60 (1H, s), 7.41 (1H, d, J = 8.0 Hz), 7.23-7.31 (3H, m), 7.05-7.13 (2H, m), 6.93 (1H, dd, J = 8.4, 1.6 Hz), 6.75 (1H, dd, J = 8.4, 1.6 Hz), 6.69 (1H, t, J = 5.6 Hz), 6.42 (1H, dd, J = 16.8, 1.6 Hz), 6.21-6.31 (1H, m), 5.75 (1H, d, J = 10.4), 4.78-4.88 (2H, m), 4.68 (2H, d, J = 6.0 Hz), 2.98-3.09 (1H, m), 2.72-2.85 (2H, m), 2.39-2.49 (1H, m), 2.31 (6H, s), 1.82-1.88 (2H, m), 1.34-1.47 (2H, m), 1.28 (6H, d, J = 6.8 Hz); LCMS: 94.2%, MS (ESI): m/z 55.3 [M + H]+.
15		yellow powder; 1H-NMR (CDCl3, 400 MHz): δ 8.18 (1H, s), 7.80 (1H, brs), 7.62 (1H, s), 7.27-7.32 (2H, m), 7.07-7.11 (2H, m), 6.92-7.05 (2H, m), 6.69-6.74 (2H, m), 6.24 (1H, d, J = 15.2 Hz), 4.67-4.76 (4H, m), 3.20-3.21 (2H, m), 3.01- 3.04 (2H, m), 2.88-2.94 (2H, m), 2.33 (6H, s), 1.98-2.01 (2H, m), 1.36-1.45 (2H, m), 1.28 (6H, d, J = 6.8 Hz); LCMS: 95.4%, MS (ESI): m/z 618.3 [M + H]+.
16		yellow powder; 1H-NMR (CDCl3, 400 MHz): δ 9.22 (1H, brs), 8.59 (1H, t, J = 5.8 Hz), 8.42 (1H, d, J = 7.6 Hz), 8.19 (1H, s), 7.70 (1H, s), 7.66 (1H, d, J = 6.8 Hz), 7.40-7.47 (4H, m), 7.16-7.20 (1H, m), 7.04-7.08 (1H, m), 6.61 (1H, d, J = 15.2 Hz), 4.83-4.88 (2H, m), 4.58 (2H, d, J = 6.0 Hz), 3.38-3.40 (1H, m), 3.27 (2H, d, J = 6.4 Hz), 2.98-3.05 (3H, m), 2.56 (6H, s), 2.21-2.38 (2H, m), 1.65-1.68 (2H, m), 1.25-1.29 (8H, m); LCMS: 95.6%, MS (ESI): m/z 608.3 [M + H]+.
17		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 11.13 (1H, brs), 10.76 (1H, brs), 9.08 (1H, brs), 8.24 (1H, d, J = 6.0 Hz), 8.00-8.22 (3H, m), 7.79 (1H, s), 7.73 (1H, s), 7.43 (1H, d, J = 8.0 Hz), 7.33 (1H, d, J = 7.2 Hz), 7.23 (1H, s), 7.05-7.15 (1H, m), 6.80-6.90 (1H, m), 6.73 (1H, d, J = 3.6 Hz), 6.56 (1H, d, J = 16.0 Hz), 4.55-4.70 (4H, m), 3.85-3.95 (2H, m), 2.85-3.00 (4H, m), 2.74 (6H, d, J = 3.6 Hz), 1.85- 2.00 (2H, m), 1.30-1.50 (2H, m), 1.22 (6H, d, J = 6.4 Hz); LCMS: 100%, MS (ESI): m/z 607.3 [M + Na]+
18		Racemic mixture; white powder; 1H-NMR (CDCl3, 400 MHz): δ 7.61 (1H, s), 7.24 (1H, t, J = 7.8 Hz), 6.88-6.96 (3H, m), 6.78-6.81 (1H, m), 6.60-6.65 (1H, m), 6.40-6.45 (1H, m), 4.69-4.76 (4H, m), 4.48-4.51 (1H, m), 3.83-3.90 (1H, m), 3.43-3.72 (3H, m), 2.90-3.11 (6H, m), 2.27 (6H, d, J = 5.6 Hz), 1.99-2.08 (4H, m), 1.73-1.91 (4H, m), 1.25- 1.37 (8H, m); LCMS: 94.9%, MS (ESI): m/z 612.5 [M + Na]+.
19		white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 8.72 (1H, s), 7.87 (1H, s), 7.58 (2H, s), 7.46-7.54 (2H, m), 7.33-7.40 (2H, m), 7.18-7.26 (2H, m), 6.90-7.01 (1H, m), 6.64 (1H, brs), 6.54 (1H, s), 6.13 (1H, d, J = 15.6 Hz), 4.82 (2H, s), 4.55-4.65 (2H, m), 3.11 (2H, d, J = 5.2 Hz), 2.98-3.05 (1H, m), 2.79-2.88 (3H, m), 2.28 (6H, s), 1.70-1.80 (2H, m), 1.29 (8H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 629.2 [M + Na]+
20		yellow powder; 1H NMR (DMSO-d6, 400 MHz): δ 10.08 (1H, brs), 8.89 (1H, t, J = 5.6 Hz), 8.69 (1H, d, J = 7.6 Hz),, 8.50 (1H, d, J = 8.4 Hz), 7.88 (1H, d, J = 8.4 Hz), 7.60-7.85 (7H, m), 7.43-7.49 (2H, m), 6.73-6.80 (1H, m), 6.50 (1H, d, J = 16.0 Hz), 5.04 (2H, d, J = 6.4 Hz), 4.30- 4.33 (2H, m), 3.11-3.17 (1H, m), 3.00 (2H, d, J = 6.4 Hz), 2.83-2.92 (1H, m), 2.62-2.67 (2H, m), 2.11 (6H, s), 1.71- 1.75 (2H, m), 1.07-1.27 (8H, m); LCMS: 100%, MS (ESI): m/z 619.4 [M + H]+.
21		Racemic mixture; white powder: 1H-NMR (CDCl3, 400 MHz): δ 7.60 (1H, s), 7.12 (1H, t, J = 7.2 Hz), 6.82-6.93 (1H, m), 6.64-6.69 (1H, m), 6.60-6.63 (1H, m), 6.40-6.52 (3H, m), 4.70-4.80 (2H, m), 4.56-4.70 (2H, m), 3.37-3.83 (6H, m), 2.89-3.16 (6H, m), 2.25-2.31 (6H, m), 1.93-2.01 (3H, m), 1.59-1.76 (2H, m), 1.39-1.48 (2H, m), 1.23-1.33 (8H, m); LCMS: 100%, MS (ESI): m/z 611.5 [M + Na]+.
22		Racemic mixture; white powder; 1H-NMR (DMSO-d6, 400 MHz): δ 7.89 (1H, brs), 7.59 (1H, s), 7.42-7.56 (2H, m), 7.21-7.26 (1H, m), 7.06 (1H, t, J = 6.0 Hz), 6.83-6.92 (1H, m), 6.65-6.75 (1H, m), 6.40 (1H, d, J = 15.6 Hz), 4.65-4.77 (4H, m), 3.86-4.03 (1H, m), 3.75-3.85 (1H, m), 3.63 (1H, t, J = 5.6 Hz), 3.42-3.53 (1H, m), 3.18-3.36 (1H, m), 2.88- 3.12 (6H, m), 2.32-2.46 (1H, m), 2.20-2.30 (7H, m), 1.83- 1.92 (2H, m), 1.54-1.82 (2H, m), 1.19-1.40 (10H, m); LCMS: 100%, MS (ESI): m/z 617.5 [M + H]+.
23		white powder; 1H NMR (DMSO-d6, 400 MHz): δ 11.52 (1H, brs), 9.98 (1H, brs), 9.01 (1H, t, J = 5.4 Hz), 8.00 (1H, s), 7.91 (1H, s), 7.77 (1H, s), 7.73 (1H, d, J = 7.2 Hz ), 7.39 (1H, t, J = 8.0 Hz), 7.31-7.34 (2H, m), 7.26 (1H, d, J = 8.0 Hz), 6.83 (1H, s), 6.67-6.73 (1H, m), 6.33 (1H, d, J = 15.2 Hz), 4.63-4.67 (4H, m), 3.13-3.19 (3H, m), 2.86- 2.94 (3H, m), 2.26 (6H, s), 1.85-1.91 (2H, m), 1.29-1.36 (2H, m), 1.23 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 607.3 [M + H]+.
24		brown powder; 1H-NMR (DMSO-d6, 400 MHz): δ 10.2 (1 (2H, m), 2.85-2.93 (2H, m), 2.72-2.83 (2H, m), 2.17-2.35 (6H, m), 1.81-1.90 (2H, m), 1.14-1.34 (8H, m); LCMS: 96.5 %, MS (ESI): m/z = 608.3 [M + H]+.
25		white powder; 1H-NMR (CDCl3, 400 MHz): δ 10.44 (1H, brs), 7.61 (1H, brs), 7.54-7.63 (3H, m), 7.48 (1H, d, J = 7.6 Hz), 7.32-7.41 (2H, m), 6.93-7.07 (2H, m), 6.79 (1H, d, J = 7.2 Hz), 6.57-6.68 (2H, m), 6.21 (1H, d, J = 14.8 Hz), 4.90 (2H, d, J = 5.6 Hz), 4.58-4.68 (2H, m), 3.12 (2H, d, J = 5.6 Hz), 3.98-3.06 (1H, m), 2.80-2.91 (3H, m), 2.29 (6H, s), 1.74-1.84 (2H, m), 1.29 (6H, d, J = 6.8 Hz), 1.20-1.26 (2H, m); LCMS: 100%, MS (ESI): m/z 629.3 [M + Na]+.
26		(3R, 4R); pale-yellow powder; 1H NMR (400 MHz, DMSO- d6): δ 10.91-11.17 (2H, m), 9.03 (1H, br s), 8.82 (1H, br s), 8.38-8.58 (3H, m), 7.79-7.89 (1H, m), 7.70-7.77 (1H, m), 7.62-7.67 (1H, m), 7.50-7.57 (2H, m), 7.42-7.49 (1H, m), 7.37 (1H, br d, J = 7.2 Hz), 6.85-6.98 (1H, m), 6.63 (1H, d, J = 15.6 Hz), 5.67-5.96 (1H, m), 4.33-4.50 (2H, m), 3.96 (2H, d, J = 6.8 Hz), 3.42-3.57 (2H, m), 2.97-3.25 (3H, m), 2.81-2.90 (1H, m), 2.77 (6H, s), 2.58-2.69 (1H, m), 1.39- 1.90 (3H, m), 1.19 (6H, br d, J = 6.4 Hz); LCMS: 100%, MS (ESI): m/z 649.3 [M + H]+
27		(1R, 4R); yellow powder; 1H-NMR (400 MHz, CD3OD): δ 8.67 (1H, s), 8.42 (1H, br d, J = 6.4 Hz), 8.24 (1H, br d, J = 6.4 Hz), 7.84-7.93 (2H, m), 7.78 (1H, d, J = 9.2 Hz), 7.68 (1H, br s), 7.49-7.62 (3H, m), 6.95-7.10 (1H, m), 6.72 (1 H, br d, J = 15.2 Hz), 4.70-5.10 (2H, m), 4.07 (2H, br d, J = 6.8 Hz) 3.47-3.65 (2H, m), 2.91-3.01 (6H, m), 2.77-2.87 (1H, m), 1.87-2.10 (3H, m), 1.65-1.72 (1H, m), 1.30-1.51 (4H, m), 1.12-1.23 (6H, m); LCMS: 100%, MS (ESI): m/z 634.3 [M + H]+.
28		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.42 (1H, s), 8.37 (1H, d, J = 6.0 Hz), 7.68-7.77 (2H, m), 7.61-7.67 (1H, m), 7.46-7.60 (4H, m), 7.40 (1H, d, J = 7.6 Hz), 6.92- 7.02 (1H, m), 6.64 (1 H, d, J = 15.2 Hz), 5.01-5.04 (1H, m), 4.39-4.43 (1H, m), 4.06 (2H, d, J = 6.4 Hz), 3.65 (2H, t, J = 6.0 Hz), 3.33-3.41 (2H, m), 2.97 (6H, s), 2.82-2.91 (1H, m), 1.74-1.80 (2H, m), 1.15-1.25 (6H, m); LCMS: 100%, MS (ESI): m/z 594.3 [M + H]+.
29		yellow solid; 1H-NMR (400 MHz, CD3OD): δ 8.66 (1H, s), 6.42-6.44 (1H, m), 8.21-8.23 (1H, m), 7.80-7.87 (3H, m), 7.59-7.71 (4H, m), 7.00-7.07 (1H, m), 6.74-6.78 (1H, d, J = 15.6 Hz), 4.95-5.02 (1H, m), 4.71-4.81 (1H, m), 4.31-3.41 (2H, m), 4.08 (2H, d, J = 7.2 Hz), 3.46-3.47 (2H, m), 3.08- 3.13 (2H, m), 2.96-2.97 (6H, m), 1.85-1.97 (2H, m), 1.29- 1.38 (2H, m), 1.16-1.19 (6H, m); LCMS: 100.0%, MS (ESI): 634.3 m/z [(M + H)]+.
30		Racemic mixture; off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.27-8.42 (2H, m) 7.25-7.75 (8H, m), 6.91-7.07 (1H, m), 6.33 (1H, d, J = 15.2 Hz), 4.80-4.87 (1H, m), 4.60- 4.67 (2H, m), 4.28-4.37 (1H, m), 3.47-3.56 (1H, m), 3.26 (2H, d, J = 6.4 Hz), 3.05-3.13 (1H, m), 2.85-2.92 (1H, m), 2.45-2.54 (2H, m), 2.36 (6H, s), 2.01-2.11 (1H, m), 1.65- 1.75 (2H, m), 1.15-1.26 (6H, m); LCMS: 95.9%, MS (ESI): m/z 324.2 [M/2 + H]+.
31		light yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.32 (1H, d, J = 6.0 Hz), 8.29 (1H, s), 7.63-7.68 (1H, m), 7.53-7.61 (2H, m), 7.49 (1H, t, J = 6.8 Hz), 7.36-7.40 (2H, m), 7.31-7.35 (2H, m), 6.91-7.00 (1H, m), 6.38-6.42 (1H, m), 4.34-4.38 (1H, m), 4.13-4.25 (2H, m), 3.74-3.82 (1H, m), 3.49 (2H, d, J = 6.8 Hz), 2.98-3.13 (2H, m), 2.85 (1H, m), 2.53 (6H, s), 1.81 (2H, m), 1.23-1.45 (3H, m), 1.19 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 620.2 [M + H]+.
32		(1S, 3S); light yellow solid; 1H-NMR (MeOD, 400 MHz): δ 8.69-8.71 (1H, m), 8.42-8.45 (1H, m), 8.25-8.27 (1H, m), 7.80-7.88 (3H, m), 7.58-7.72 (4H, m), 6.99-7.07 (1H, m), 6.73 (1H, d, J = 15.2 Hz), 5.01-5.06 (1H, m), 4.91-4.94 (1H, m), 4.71-4.78 (1H, m), 4.39-4.44 (1H, m), 4.26-4.29 (1H, m), 4.07 (2H, d, J = 7.2 Hz), 2.96 (6H, s), 2.84-2.88 (1H, m), 2.06-2.32 (2H, m), 1.95-1.99 (1H, m), 1.61-1.80 (3H, m), 1.18-1.21 (6H, m); LCMS: 99.7%, MS (ESI): 620.2 m/z [M + H]+.
33		(1R, 4R); white powder; 1H NMR (CD3OD, 400 MHz): δ 8.66 (1H, d, J = 2.0 Hz), 8.43 (1H, d, J = 6.8 Hz), 8.23 (1H, d, J = 6.8 Hz), 7.76-7.88 (3H, m), 7.66-7.74 (1H, m), 7.55-7.63 (3H, m), 6.97-7.08 (1H, m), 6.71 (1H, d, J = 15.6 Hz), 4.89-4.90 (2H, m), 4.07 (2H, d, J = 6.4 Hz), 3.45-3.54 (1H, m), 3.17-3.26 (1H, m), 3.04 (1H, m), 2.96 (6H, s), 2.84 (1H, m), 1.88-2.05 (2H, m), 1.67-1.83 (2H, m), 1.36-1.49 (1H, m), 1.28-1.35 (1H, m), 1.14-1.21 (7H, m), 0.84-1.11 (2H, m); LCMS: 99.7%, MS (ESI): m/z 648.2 [M + H]+; HPLC (254 nm): 100%.
34		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.67 (1H, s), 8.38-8.45 (1H, br s), 8.18-8.26 (1H, m), 7.78-7.88 (3H, m), 7.55-7.73 (4H, m), 6.97-7.08 (1H, m), 6.74 (1H, d, J = 15.2 Hz), 4.95-5.03 (1H, m), 4.66-4.76 (1H, m), 4.48-4.59 (2H, m), 4.07 (2H, d, J = 6.8 Hz), 3.39-3.54 (1H, m), 3.03- 3.24 (3H, m), 2.96 (6H, s), 2.76 (3H, s), 2.14-2.31 (2H, m), 1.46-1.80 (2H, m), 1.19 (6H, d, J = 6.8 Hz); LCMS: 99.7%, MS (ESI): m/z 633.3 [M + H]+
35		light yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.69 s), 8.44 (1H, d, J = 6.4 Hz), 8.23 (1H, d, J = 6.8 Hz), 7.81-7.87 (3H, m), 7.68-7.72 (2H, m), 7.59-7.60 (2H, m), 6.99-7.07 (1H, m), 6.73 (1H, d, J = 15.2 Hz), 5.04-5.08 (1H, m), 4.70-4.74 (1H, m), 4.07 (2H, d, J = 6.4 Hz), 3.41-3.44 (2H, m), 2.96 (6H, s), 2.82-2.86 (1H, m), 1.69- 1.73 (2H, m), 1.28 (6H, s), 1.21 (6H, d, J = 6.8 Hz); LCMS: 98.2%, MS (ESI): 622.3 m/z [(M + H)]+.
36		White solid; 1H NMR (400 MHz, DMSO-d6): δ 11.24-11.45 (2H, m), 9.42-9.66 (1H, m), 8.61-8.66 (1H, m), 8.41-8.47 (1H, m), 8.18-8.23 (1H, m), 7.72-7.75 (2H, m), 7.67-7.69 (1H, m), 7.54-7.60 (1H, m), 7.41-7.52 (2H, m), 6.91-7.01 (1H, m), 6.65 (1H, m), 4.74-4.83 (1H, m), 4.50-4.61 (1H, m), 3.95-4.02 (2H, m), 2.72-2.81 (6H, m), 1.76-1.91 (1H, m), 1.44-1.68 (5H, m), 1.21-1.38 (2H, m), 1.10-1.16 (6H, m); LCMS: 100%, MS (ESI): m/z 634.3 [M + H]+.
37		Racemic mixture; off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.64-8.70 (1H, m), 8.40-8.51 (1H, m), 8.17-8.28 (1H, m), 7.81-7.92 (3H, m), 7.68-7.75 (2H, m), 7.58-7.66 (2H, m), 7.01-7.09 (1H, m), 6.77 (1H, d, J = 15.2 Hz), 5.11- 5.20 (1H, m), 4.53-4.72 (2H, m), 4.09 (2H, d, J = 7.2 Hz), 3.38-3.86 (4H, m), 3.08-3.21 (1H, m), 2.93 (6H, s), 2.03- 2.32 (2H, m), 1.14-1.26 (6H, m); HPLC: 100%, MS (ESI): m/z 606.2 [M + H]+.
38		Racemic mixture; light yellow solid; 1H-NMR (MeOD, 400 MHz): δ 8.67 (1H, s), 8.41-8.43 (1H, m), 8.18-8.23 (1H, m), 7.80-7.87 (3H, m), 7.59-7.68 (4H, m), 6.99-7.07 (1H, m), 6.74 (1H, d, J = 15.2 Hz), 4.95-4.99 (1H, m), 4.72-4.81 (1H, m), 4.07 (2H, d, J = 7.2 Hz), 3.42-3.93 (4H, m), 3.09- 3.14 (1H, m), 2.96 (6H, s), 2.07-2.22 (1H, m), 1.43-1.98 (5H, m), 1.16-1.19 (6H, m); LCMS: 99.8%, MS (ES1): 634.2 m/z [(M + H)]+
39		Light yellow solid; 1H NMR (400 MHz, CD3OD): δ 8.68 (1H, s), 8.42 (1H, d, J = 6.0 Hz), 8.21 (1H, d, J = 6.4 Hz), 7.82-7.89 (3H, m), 7.65-7.75 (2H, m), 7.59-7.64 (2H, m), 7.00-7.11 (1H, m), 6.74 (1H, d, J = 15.6 Hz), 4.98-5.07 (1H, m), 4.68-4.75 (1H, m), 4.54-4.62 (2H, m), 4.07 (2H, d, J = 6.8 Hz), 3.59-3.69 (1H, m), 3.08-3.28 (3H, m), 2.98 (6H, s), 2.94 (6H, s), 2.21-2.29 (2H, m), 1.72-1.87 (2H, m), 1.29- 1.33 (2H, m), 1.19-1.24 (6H, m); LCMS: 97.9%, MS (ESI): m/z 647.3 [M + H]+
40		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.58 (1H, s), 8.38 (1H, s), 8.10-8.19 (1H, m), 7.80-7.90 (2H, m), 7.66- 7.74 (2H, m), 7.52-7.63 (3H, m), 6.02 (1H, s), 5.00-5.09 (1H, m), 4.65-4.72 (1H, m), 4.48-4.56 (2H, m), 3.46-3.59 (1H, m), 2.97-3.23 (3H, m), 2.33 (3H, s), 2.10-2.22 (2H, m), 2.01 (3H, s), 1.47-1.76 (2H, m), 1.21 (6H, d, J = 6.8 Hz); HPLC: 96.1%, MS (ESI): m/z 590.2 [M + H]+
41		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.51 (1H, s), 8.37 (1H, d, J = 2.8 Hz), 8.11 (1H, d, J = 6.8 Hz), 7.77- 7.89 (4H, m), 7.62-7.71 (3H, m), 7.57 (1H, d, J = 6.8 Hz), 6.97-7.05 (1H, m), 6.58-6.63 (2H, m), 5.03-5.10 (1H, m), 4.76-4.81 (1H, m), 4.74 (2H, s), 4.09 (2H, d, J = 7.2 Hz), 3.08-3.17 (1H, m), 2.99 (6H, s), 1.29-1.34 (6H, m); LCMS: 99.2%, MS (ESI): 617.2 m/z [M + H]+
42		off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.65 (1H, d, J = 1.6 Hz), 8.41 (1H, d, J = 6.8 Hz), 8.21 (1H, d, J = 6.4 Hz), 7.77-7.89 (3H, m), 7.55-7.73 (4H, m), 6.97- 7.12 (1H, m), 6.75 (1 H, d, J = 15.2 Hz), 4.97-5.03 (1H, m), 4.69-4.76 (1H, m), 4.07 (2H, d, J = 6.8 Hz), 3.66- 3.85 (8H, m), 3.04-3.16 (1H, m), 2.96 (6 H, s), 1.16-1.21 (6H, m); HPLC: 99.4%, MS (ESI): m/z 606.2 [M + H]+
43		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.70 (1H, s), 8.46 (1H, d, J = 7.2 Hz), 8.22-8.28 (1H, m), 7.82-7.89 (3H, m), 7.57-7.76 (4H, m), 7.00-7.09 (1H, m), 6.71 (1H, d, J = 15.2 Hz), 4.96-5.02 (1H, m), 4.75-4.83 (1H, m), 4.08 (2H, d, J = 6.4 Hz), 3.84-4.01 (2H, m), 3.32-3.39 (2H, m), 3.23-3.28 (1H, m), 3.06-3.21 (1H, m), 2.98 (6H, s), 2.83- 2.88 (1H, m), 1.73-1.80 (1H, m), 1.55-1.64 (2H, m), 1.25- 1.32 (1H, m), 1.18-1.24 (6H, m); LCMS: 100%, MS (ESI): m/z 634.2 [M + H]+
44		Light yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.88- 6.89 (1H, m), 8.41-8.43 (1H, m), 8.26-8.28 (1H, m), 7.78- 7.88 (3H, m), 7.67-7.71 (1H, m), 7.55-7.60 (3H, m), 6.99- 7.07 (1H, m), 6.71 (1H, d, J = 15.2 Hz ), 4.95-4.99 (1H, m), 4.78-4.82 (1H, m), 4.07 (2H, d, J = 7.2 Hz), 3.52-3.57 (1H, m), 3.40 (3H, s), 3.22-3.28 (1H, m), 2.96 (6H, s), 2.80-2.87 (1H, m), 2.03-2.17 (3H, m), 1.71-1.73 (1H, m), 1.27-1.48 (4H, m), 1.16-1.19 (6H, m); LCMS: 100.0%, MS (ESI): 648.3 m/z [(M + H)]+
45		Light yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.68 (1H, s), 8.45 (1H, d, J = 6.4 Hz), 8.23 (1H, d, J = 6.8 Hz), 7.82-7.83 (3H, m), 7.68-7.72 (1H, m), 7.59-7.65 (3H, m), 6.99-7.05 (1H, m), 6.72 (1H, d, J = 15.2 Hz), 5.04-5.08 (1H, m), 4.77-4.81 (1H, m), 4.07 (2H, d, J = 6.8 Hz), 3.37-3.48 (3H, m), 3.18-3.27 (1H, m), 2.96-3.02 (8H, m), 2.83-2.88 (1H, m), 1.93-1.96 (m, 3H), 1.49-1.55 (2H, m), 1.18-1.21 (6H, m); LCMS: 100.0%, MS (ESI): 633.3 m/z [(M + H)]+
46		off-white powder: 1H NMR (400 MHz, CD3OD): δ 8.59 (1 H, d, J = 2.0 Hz), 8.38 (1H, d, J = 6.4 Hz), 8.16 (1H, d, J = 6.4 Hz), 7.79-7.88 (2H, m), 7.66-7.78 (2H, m), 7.57-7.62 (2H, m), 7.53 (1H, s), 6.51-6.58 (2H, m), 5.94 (1H, dd, J = 8.0, 3.6 Hz), 4.98-5.09 (1H, m), 4.65-4.74 (1H, m), 4.49- 4.57 (2H, m), 3.43-3.54 (1H, m), 2.95-3.21 (3H, m), 2.04- 2.21 (2H, m), 1.44-1.76 (2H, m), 1.20 (6H, d, J = 6.8 Hz); HPLC: 100%, MS (ESI): m/z 562.2 [M + H]+.
47		Light yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.43 (1H, s), 8.39 (1H, d. J = 6.4 Hz), 8.17 (1H, d, J = 6.4 Hz), 7.78-7.84 (2H, m), 7.62-7.71 (2H, m), 7.56-7.62 (2H, m), 7.55 (1H, s), 4.91-5.05 (1H, m), 4.63-4.71 (1H, m), 4.47- 4.551 (2H, m), 3.43-3.56 (1H, m), 3.10-3.29 (2H, m), 3.00- 3.08 (1H, m), 2.02-2.21 (5H, m), 1.63-1.76 (1H, m), 1.51- 1.59 (1H, m), 1.21-1.27 (6H, m); LCMS: 96.8%, MS (ESI): m/z 574.2 [M + H]+
48		Pale yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.55 (1H, d, J = 2.0 Hz), 8.37-8.42 (1H, m), 8.20 (1H, d, J = 6.4 Hz), 7.77-7.92 (3H, m), 7.64-7.72 (1H, m), 7.54-7.62 (3H, m), 5.98 (1H, s), 5.71 (1H, d, J = 1.2 Hz), 4.99-5.07 (1H, m), 4.67-4.73 (1H, m), 4.47-4.54 (1H, m), 3.44-3.56 (1H, m), 3.17-3.24 (1H, m), 3.03-3.09 (1H, m), 2.08-2.21 (2H, m), 2.06 (3H, s), 1.64-1.78 (1H, m), 1.55-1.60 (1H, m), 1.16-1.21 (6H, m); LCMS; 100%. MS (ESI): m/z 576.2 [M + H]+
49		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.48 (1H, d, J = 1.6 Hz), 8.40 (1H, d, J = 6.8 Hz), 8.19 (1H, d, J = 6.8 Hz), 7.80-7.89 (3H, m), 7.63-7.72 (2H, m), 7.55-7.62 (2H, m), 4.98-5.07 (1H, m), 4.68-4.75 (1H, m), 4.51-4.57 (2H, m), 3.46-3.52 (1H, m), 3.13-3.23 (2H, m), 3.04-3.09 (1H, m), 2.08-2.17 (2H, m), 1.74-1.87 (4H, m), 1.55-1.72 (2H, m), 1.23-1.28 (6H, m); LCMS: 99.8%, MS (ES1): 601.2 m/z [M + H]+
50		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.57 (1H, d, J = 2.0 Hz), 8.41 (1H, d, J = 6.4 Hz), 8.19 (1H, d, J = 6.8 Hz), 7.73-7.88 (3H, m), 7.66-7.71 (1H, m), 7.56-7.62 (3H, m), 7.06-7.17 (1H, m), 6.25 (1H, dd, J = 14.8, 2.0 Hz), 4.99-5.06 (1H, m), 4.66-4.73 (1H, m), 4.45-4.52 (2H, m), 3.47-3.58 (1H, m), 3.18-3.38 (2H, m, overlap with CD3OD signal), 3.0-3.09 (1H, m), 2.10-2.19 (2H, m), 1.98 (3H, dd, J = 6.8, 1.6 Hz), 1.65-1.80 (1H, m), 1.49- 1.64 (1H, m), 1.18 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 576.3 [M + H]+
51		Racemic mixture; off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.71 (1H, s), 8.48 (1H, d, J = 6.4 Hz), 8.27 (1H, d, J = 6.0 Hz), 7.81-7.92 (3H, m), 7.56-7.75 (4H, m), 7.00- 7.13 (1H, m), 6.77 (1H, d, J = 15.2 Hz), 5.06-5.14 (1H, m), 4.72-4.79 (1H, m), 4.06-4.21 (3H, m), 3.86-3.97 (2H, m), 3.43-3.59 (2H, m), 3.25-3.33 (3H, m), 3.14-3.26 (1H, m), 2.98 (6H, s), 2.83-2.94 (1H, m), 1.57-1.82 (2H, m), 1.21 (6H, d, J = 6.4 Hz); HPLC: 100%, MS (ESI): m/z 649.3 [M + H]+
52		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.69 (1H, s), 8.47 (1H, s), 8.26 (1H, d, J = 5.2 Hz), 7.80-7.93 (3H, m), 7.56-7.76 (4H, m), 7.02-7.14 (1H, m), 6.76 (1H, d, J = 14.8 Hz), 5.08-5.18 (1H, m), 4.69-4.78 (1H, m), 4.47- 4.56 (2H, m), 4.03-4.08 (2H, m), 3.48-3.68 (5H, m), 2.94-3.18 (3H, m), 2.11-2.23 (2H, m), 2.00-2.07 (2H, m), 1.80-1.92 (4H, m), 1.51-1.67 (2H, m), 1.20 (6H, d, J = 6.0 Hz); HPLC: 97.1%, MS (ESI): m/z 659.3 [M + H]+
53		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.69 (1H, s), 8.45 (1H, d, J = 5.2 Hz), 8.25 (1H, d, J = 6.4 Hz), 7.81- 7.96 (3H, m), 7.59-7.76 (4H, m), 7.02-7.17 (1H, m), 6.79 (1H, d, J = 15.2 Hz), 5.01-5.08 (1H, m), 4.73-4.78 (1H, m), 4.48-4.55 (2H, m), 4.05-4.21 (4H, m), 3.79-3.92 (2H, m), 3.48-3.63 (4H, m), 3.12-3.28 (4H, m), 2.11-2.27 (2H, m), 1.56-1.85 (2H, m), 1.20 (6H, d, J = 6.0 Hz); HPLC: 100%, MS (ESI): m/z 661.3 [M + H]+
54		off-white powder; 1H NMR (CD3OD, 400 MHz): δ 8.56 (1H, s), 8.31-8.36 (1H, m), 8.08-8.13 (1H, m), 7.77-7.90 (2H, m), 7.42-7.75 (5H, m), 7.06-7.13 (1H, m), 6.46 (1H, d, J = 15.2 Hz), 4.64-4.71 (1H, m), 4.52-4.58 (2H, m), 4.14- 4.23 (2H, m), 3.44-3.53 (4H, m), 2.87-3.19 (3H, m), 2.04- 2.13 (2H, m), 1.29-1.72 (3H, m), 1.20 (6H, d, J = 6.8 Hz); LCMS: 99.8%, MS (ESI): 606.2 m/z [M + H]+
55		yellow powder; 1H NMR (400 MHz, DMSO-d6): δ ppm 10.95 (1H, brs) 8.87 (1H, d, J = 4.8 Hz), 8.65-8.72 (1H, m), 8.64 (1H, s), 8.13 (2H, brs), 7.65-7.75 (2H, m), 7.39-7.57 (3H, m), 7.24-7.38 (3H, m), 6.82-6.95 (1H, m), 6.62 (1H, d, J = 14.8 Hz), 4.18-4.48 (4H, m), 3.76-3.88 (2H, m), 3.19- 3.26 (1H, m), 2.83-2.94 (1H, m), 2.55-2.76 (9H, m), 1.86 (2H, m), 1.28-1.39 (2H, m), 1.20 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 619.3 [M + H]+
56		yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.70-8.72 (1H, m), 8.29-8.33 (1H, m), 7.78 (1H, s), 7.61-7.72 (3H, m), 7.42-7.48 (2H, m), 7.32-7.34 (1H, m), 6.86-6.92 (1H, m), 6.72-6.75 (1H, m), 4.32-4.36 (2H, m), 4.03 (2H, d, J = 7.2 Hz), 3.45-3.49 (1H, m), 3.02-3.15 (3H, m), 2.94 (6H, s), 2.61 (3H, s), 2.09-2.12 (2H, m), 1.55- 1.61 (2H, m), 1.26 (6H, d, J = 6.8 Hz); LCMS: 100.0%, MS (ES1): 633.3 m/z [(M + H)]+
57		off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.63 (1H, s), 8.32-8.37 (1H, m), 8.14 (1H, d, J = 6.4 Hz), 7.80- 7.87 (2H, m), 7.72-7.76 (1H, m), 7.68 (1H, t, J = 8.0 Hz), 7.54-7.63 (2H, m), 7.48 (1H, s), 6.96-7.15 (1H, m), 6.72 (1H, d, J = 15.20 Hz), 4.66-4.73 (2H, m), 4.53-4.59 (2H, m), 4.16 (2H, d, J = 6.8 Hz), 3.69-3.74 (2H, m), 3.42-3.53 (1H, m), 2.93-3.25 (5H, m), 2.03-2.32 (6H, m), 1.43-1.69 (2H, m), 1.20 (6H, d, J = 7.2 Hz); HPLC: 100%, MS (ESI): m/z 645.3 [M + H]+
58		yellow powder; 1H NMR (400 MHz, CD3OD): δ 8.63 (1H, s), 8.37 (1H, d, J = 6.4 Hz), 8.16 (1H. d, J = 6.2 Hz), 7.73- 7.88 (3H, m), 7.50-7.71 (4H, m), 6.95-7.08 (1H, m), 6.72 (1H, d, J = 15.2 Hz), 4.95-5.03 (1H, m), 4.65-4.71 (1H, m), 4.46-4.54 (2H, m), 3.99-4.19 (4H, m), 3.42-3.50 (1H, m), 3.10-3.17 (2H, m), 2.91-3.07 (4H, m), 2.05-2.13 (2H, m), 1.43-1.74 (2H, m), 1.16 (6H, d, J = 6.8 Hz); HPLC: 100%, MS (ESI): m/z 662.3 [M + H]+
59		pale yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.61 (1H, d, J = 1.6 Hz), 8.33 (1H, d, J = 6.8 Hz), 8.11 (1H, d, J = 6.4 Hz), 7.77-7.85 (2H, m), 7.72-7.76 (1H, m), 7.64- 7.70 (1H, m), 7.54-7.63 (2H, m), 7.48 (1H, s), 6.97-7.07 (1H, m), 6.72 (1H, d, J = 15.2 Hz), 4.96-5.03 (2H, m), 4.67-4.74 (1H, m), 4.05-4.09 (2H, m), 3.91-4.00 (4H, m), 3.26-3.32 (4H, m), 2.94-2.99 (7H, m), 1.20 (6H, d, J = 7.2 Hz); LCMS: 100%, MS (ESI): m/z 605.6 [M + H]+
60		(3R, 4R); off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.54 (1H, s), 8.33-8.37 (1H, m), 8.06-8.12 (1H, m), 7.67- 7.78 (2H, m), 7.51-7.64 (3H, m), 7.44-7.50 (2H, m), 6.38- 6.44 (2H, m), 5.80-5.86 (1H, m), 4.94-5.05 (2H, m), 4.52- 4.72 (2H, m), 3.49-3.75 (2H, m), 3.32-3.38 (1H, m), 2.64- 2.95 (3H, m), 1.85-2.01 (1H, m), 1.71-1.79 (1H, m), 1.42- 1.50 (1H, m), 1.09 (6H, d, J = 6.8 Hz); HPLC: 97.5%, MS (ESI): m/z 592.3 [M + H]+
61		pale yellow powder: 1H NMR (400 MHz, CD3OD): δ 8.64 (1H, s), 8.37 (1H, d, J = 6.8 Hz), 8.16 (1H, d, J = 6.8 Hz), 7.76-7.86 (3H, m), 7.65-7.70 (1H, m), 7.54-7.64 (3H, m), 6.98-7.07 (1H, m), 6.72 (1H, d, J = 15.2 Hz), 4.95-5.01 (1H, m), 4.81-4.87 (1H, m), 4.68-4.74 (1H, m), 4.07 (2H, d, J = 7.2 Hz), 3.85-3.99 (2H, m), 3.52-3.64 (3H, m), 3.40 (3H, s), 3.00-3.09 (1H, m), 2.96 (6H, s), 2.91 (1H, s), 1.83-2.05 (3H, m), 1.57-1.69 (2H, m), 1.15-1.20 (6H, m); LCMS: 99.4%, MS (ESI): m/z 634.3 [M + H]+
62		Racemic mixture; yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.65-8.69 (1H, m), 8.43-8.47 (1H, m), 8.18-8.24 (1H, m), 7.78-7.88 (3H, m), 7.65-7.72 (2H, m), 7.57-7.61 (2H, m), 6.98-7.06 (1H, m), 6.73 (1H, d, J = 15.2 Hz), 4.99- 5.11 (2H, m), 4.70-4.81 (1H, m), 3.84-4.12 (5H, m), 3.38- 3.65 (3H, m), 2.81-3.24 (9H, m), 1.16-1.22 (6H, m); LCMS: 100%, MS (ESI): 657.2 m/z [M + Na]+
63		yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.63 (1H, s), 8.39-8.45 (1H, m), 8.11-8.17 (1H, m), 7.50-7.91 (7H, m), 6.96-7.13 (1H, m), 6.72 (1H, d, J = 15.4 Hz), 5.09-5.16 (1H, m), 3.97-4.16 (3H, m), 3.37-3.62 (3H, m), 3.12-3.27 (1H, m), 2.77-3.05 (8H, m), 2.24-2.31 (1H, m), 1.68-2.05 (3H, m), 1.12-1.29 (6H, m); LCMS: 100%, MS (ESI): 619.3 m/z [M + H]+
64		(3R, 4R); yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.64-8.68 (1H, m), 8.51 (1H, dd, J = 6.4, 3.2 Hz), 8.27-8.31 (1H, m), 7.81-7.92 (3H, m), 7.65-7.72 (2H, m), 7.57-7.62 (2H, m), 5.87 (1H, dd, J = 46.0, 3.6 Hz), 5.46 (1H, dd, J = 14.8, 3.6 Hz), 5.06-5.13 (1H, m), 4.65-4.75 (1H, m), 3.69- 3.76 (1H, m), 3.54-3.62 (1H, m), 3.34-3.47 (3H, m), 2.78- 3.01 (3H, m), 1.98-2.05 (1H, m), 1.81-1.92 (1H, m), 1.53- 1.65 (1H, m), 1.20 (6H, d, J = 6.8 Hz); LCMS: 99.4%, MS (ESI): 610.2 m/z [M + H]+
65		(3R, 4R); yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.58-8.61 (1H, m), 8.44 (1H, dd, J = 6.4, 2.4 Hz), 8.17-8.22 (1H, m), 7.79-7.91 (3H, m), 7.56-7.72 (4H, m), 6.92 (1H, d, J = 2.0 Hz), 5.05-5.13 (1H, m), 4.68-4.75 (1H, m), 3.69- 3.76 (1H, m), 3.37-3.59 (4H, m), 2.60-3.01 (7H, m), 1.96- 2.07 (3H, m), 1.79-1.88 (1H, m), 1.52-1.63 (1H, m), 1.18 (6H, d, J = 6.8 Hz); LCMS: 98.3%, MS (ESI): 632.2 m/z [M + H]+
66		(3R, 4R); yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.52-8.59 (1H, m), 8.39-8.45 (1H, m), 8.04-8.13 (1H, m), 7.52-7.88 (7H, m), 5.94 (1H, s), 5.69 (1H, s), 5.08-5.17 (1H, m), 4.62-4.73 (1H, m), 3.34-3.76 (5H, m), 2.76-3.05 (3H, m), 1.52-2.10 (6H, m), 1.20 (6H, d, J = 6.8 Hz); LCMS: 98.9%, MS (ESI): 606.2 m/z [M + H]+
67		(3R, 4R); light yellow powder: 1H-NMR (CD3OD, 400 MHz): δ 8.73 (1H, d, J = 8.0 Hz), 8.32 (1H, d, J = 8.8 Hz), 7.74 (1H, s), 7.59-7.69 (3H, m), 7.46-7.48 (2H, m), 7.35- 7.37 (1H, m), 6.49-6.56 (1H, m), 6.32-6.36 (1H, m), 5.69- 5.76 (1H, m), 4.91-4.95 (3H, m), 4.84-4.86 (1H, m), 3.60- 3.66 (1H, m), 3.34-3.39 (1H, m), 3.25-3.28 (1H, m), 2.84- 2.94 (2H, m), 2.69-2.75 (1H, m), 2.57 (3H, s), 1.88-1.94 (1H, m), 1.73-1.77 (1H, m), 1.43-1.47 (1H, m), 1.26 (6H, d, J = 6.8 Hz); LCMS: 100.0%, MS (ESI): 606.3 m/z [(M + H)]+
68		(3R, 4R); yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.59-8.63 (1H, m), 8.42-8.47 (1H, m), 8.17-8.22 (1H, m), 7.55-7.73 (7H, m), 7.06-7.12 (1H, m), 6.22 (1H, d, J = 15.2 Hz), 5.05-5.12 (1H, m), 4.64-4.75 (1H, m), 3.69-3.76 (1H, m), 3.30-3.58 (4H, m), 2.89-3.01 (1H, m), 2.75-2.84 (2H, m), 1.95-2.04 (4H, m), 1.80-1.91 (1H, m), 1.52-1.63 (1H, m), 1.18 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): 606.3 m/z [M + H]+
69		Racemic mixture; yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.54-8.61 (1H, m), 8.42 (1H, d, J = 6.8 Hz), 8.14- 8.18 (1H, m), 7.55-7.87 (7H, m), 7.06-7.14 (1H, m), 6.22 (1H, d, J = 15.2 Hz), 5.03-5.13 (1H, m), 4.67-4.72 (1H, m), 3.81-4.15 (3H, m), 3.34-3.61 (3H, m), 2.79-3.25 (3H, m), 1.97 (3H, d, J = 6.8 Hz), 1.16-1.21 (6H, m); LCMS: 100%, MS (ESI): 592.3 m/z [M + H]+
70		Yellow powder; 1H-NMR (CD3OD, 400 MHz): δ 8.54 (1H, d, J = 7.6 Hz), 8.45 (1H, d, J = 8.8 Hz), 7.65-7.77 (4H, m), 7.45-7.52 (2H, m), 7.35-7.37 (1H, m), 6.91-6.97 (1H, m), 6.22 (1H, d, J = 14.8 Hz), 4.93-4.94 (2H, m), 3.64-3.65 (1H, m), 3.32-3.36 (2H, m), 3.26-3.28 (2H, m), 2.85-2.92 (2H, m), 2.74-2.77 (1H, m), 2.62 (3H, s), 1.87-1.95 (3H, m), 1.70-1.77 (1H, m), 1.44-1.52 (1H, m), 1.25 (6H, d, J = 6.8 Hz), 0.85-0.91 (1H, m); LCMS: 98.5%, MS (ESI): 620.2 m/z [(M + H)]+
71		yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.57 (1H, d, J = 2.0 Hz), 8.38 (1H, d, J = 6.8 Hz), 8.16 (1H, d, J = 6.8 Hz), 7.79-7.86 (2H, m), 7.66-7.74 (2H, m), 7.57-7.62 (3H, m), 7.07-7.14 (1H, m), 6.25 (1H, dd, J = 15.2, 1.6 Hz), 5.01-5.05 (1H, m), 4.68-4.72 (1H, m), 4.01-4.05 (4H, m), 3.33-3.36 (4H, m), 3.00-3.07 (1H, m), 1.98 (3H, dd, J = 6.8, 1.6 Hz), 1.20 (6H, dd, J = 6.8, 1.6 Hz); LCMS: 100.0%, MS (ESI): 562.2 m/z [(M + H)]+
72		(3R, 4R); yellow powder; 1H-NMR (CD3OD, 400 MHz): δ 8.46-8.52 (1H, m), 8.36-8.38 (1H, m), 8.05-8.08 (1H, m), 7.78-7.87 (2H, m), 7.65-7.69 (2H, m), 7.49-7.55 (3H, m), 7.05-7.12 (1H, m), 6.24 (1H, dd, J = 15.2, 1.2 Hz), 4.99- 5.03 (1H, m), 4.65-4.72 (1H, m), 3.67-3.73 (1H, m), 3.38- 3.48 (4H, m), 2.98-3.05 (1H, m), 2.81-2.91 (2H, m), 2.4- 2.09 (1H, m), 1.97 (3H, dd, J = 6.8, 1.2 Hz), 1.81-1.86 (1H, m), 1.62-1.68 (1H, m), 1.17-1.22 (6H, m); LCMS: 99.4%, MS (ESI): 605.3 m/z [(M + H)]+
73		(3R, 4R); off-white powder; 1H-NMR (CD3OD, 400 MHz): δ 7.85 (1H, s), 7.36-7.45 (3H, m), 7.34 (1H, d, J = 8.0 Hz), 7.19 (1H, d, J = 7.6 Hz), 6.97-7.05 (1H, m), 6.60-6.74 (1H, m), 6.17 (1H, d, J = 15.2 Hz), 4.93-4.97 (2H, m), 3.55-3.61 (1H, m), 3.45-3.54 (1H, m), 3.35-3.43 (1H, m), 3.23-3.27 (1H, m), 3.03-3.09 (1H, m), 2.94-3.01 (1H, m), 2.57-2.68 (2H, m), 2.54 (3H, s), 1.88 (3H, d, J = 6.4 Hz), 1.64-1.84 (2H, m), 1.34-1.45 (1H, m), 1.30 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 608.3 [M + H]+
74		(3R, 4R); white powder; 1H NMR (CD3OD, 400 MHz): δ 7.93 (1H, s), 7.68-7.84 (2H, m), 7.59 (2H, m), 7.36 (1H, d, J = 7.2 Hz), 7.23-7.30 (1H, m), 6.89-7.04 (2H, m), 6.77- 6.83 (1H, m), 6.48-6.56 (1H, m), 6.18 (1H, d, J = 14.8 Hz), 4.51- 4.69 (2H, m), 3.60-3.69 (2H, m), 3.41-3.52 (1H, m), 3.13- 3.19 (1H, m), 2.70-3.02 (4H, m), 1.89-1.99 (4H, m), 1.74-1.82 (1H, m), 1.41-1.57 (1H, m), 1.20-1.34 (6H, m); LCMS: 99.9%, MS (ESI): 594.2 m/z [M + H]+
75		white powder; 1H NMR (400 MHz, CDCl3): δ 8.33-8.57 (3H, m), 7.53-7.65 (4H, m), 7.34-7.48 (4H, m), 6.95-7.12 (2H, m), 6.29-6.52 (1H, m), 4.69-4.88 (1H, m), 4.38-4.59 (3H, m), 4.17-4.36 (1H, m), 3.54-3.73 (1H, m), 3.25-3.40 (2H, m), 2.83-3.05 (3H, m), 2.48 (6H, s), 1.85-2.0 (2H, m), 1.46 (9H, s), 1.24-1.26 (8H, m); LCMS: 100%, MS (ESI): m/z 719.3 [M + H]+
76		(3R, 4R); Yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.66-8.70 (1H, m), 8.45 (1H, dd, J = 6.8, 2.4 Hz), 8.19-8.24 (1H, m), 7.80-7.88 (3H, m), 7.64-7.71 (2H, m), 7.56-7.61 (2H, m), 7.01-7.08 (1H, m), 6.70 (1H, d, J = 15.2 Hz), 5.02- 5.07 (1H, m), 4.69-4.79 (1H, m), 4.02 (2H, d, J = 7.2 Hz), 3.70-3.76 (1H, m), 3.53-3.60 (3H, m), 3.31-3.46 (3H, m), 2.76-3.07 (5H, m), 1.96-2.03 (3H, m), 1.78-1.91 (4H, m), 1.51-1.62 (2H, m), 1.19 (6H, d, J = 7.2 Hz); LCMS: 100%, MS (ESI): 689.3 m/z [M + H]+.
77		Mixture of 2 trans isomer; yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.55-8.62 (1H, m), 8.41-8.46 (1H, m), 8.15- 8.19 (1H, m), 7.56-7.87 (7H, m), 7.06-7.18 (1H, m), 6.21 (1H, d, J = 16.0 Hz), 5.09-5.21 (1H, m), 4.67-4.82 (2H, m), 4.26-4.35 (1H, m), 3.41-3.62 (3H, m), 3.12-3.21 (2H, m), 2.80-2.86 (1H, m), 2.38-2.59 (1H, m), 1.97 (3H, dd, J = 7.2, 1.6 Hz), 1.18 (6H, d, J = 6.8 Hz). LCMS: 100%, MS (ESI): 592.2 m/z [M + H]+.
78		(3R, 4R); gray powder; 1H NMR (MeOD, 400 MHz): δ ppm 7.85 (1H, s), 7.34-7.48 (4H, m), 7.18 (1H, d, J = 7.6 Hz), 7.03-7.10 (1H, m), 6.49 (1H, s), 5.34-5.52 (1H, m), 5.21 (1H, dd, J = 15.2, 3.2 Hz), 4.92-4.95 (2H, m), 3.50-3.62 (2H, m), 3.37-3.45 (1H, m), 3.20-3.27 (1H, m), 2.93-3.05 (2H, m), 2.50-2.61 (5H, m), 1.67-1.83 (2 H, m), 1.33-1.42 (1H, m), 1.30 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 612.3 [M + H]+
79		Yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.56 (1H, d, J = 2.0 Hz), 8.36 (1H, d, J = 6.4 Hz), 8.15 (1H, d, J = 6.8 Hz), 7.76-7.83 (3H, m), 7.61-7.67 (1H, m), 7.53-7.60 (2H, m), 7.44 (1H, s), 5.85 (1H, dd, J = 46.0, 3.6 Hz), 5.44 (1H, dd, J = 15.2, 3.6 Hz), 5.00 (1H, d, J = 15.6 Hz), 4.63 (1H, d, J = 15.6 Hz), 3.89-4.00 (4H, m), 3.21-3.29 (4H, m, overlap with water signal), 2.87-2.95 (1H, m), 1.15-1.21 (6H, m); LCMS: 100%, MS (ESI): 566.2 m/z [M + H]+
80		Racemic mixture; Yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.62-8.65 (1H, m), 8.44-8.49 (1H, m), 8.20-8.24 (1H, m), 7.79-7.90 (3H, m), 7.65-7.71 (2H, m), 7.54-7.61 (2H, m), 5.85 (1H, dd, J = 46.4, 3.6 Hz), 5.44 (1H, dd, J = 14.8, 3.6 Hz), 5.03-5.13 (1H, m), 4.65-4.76 (1H, m), 3.81- 4.12 (3H, m), 3.32-3.61 (3H, m), 2.78-3.21 (4H, m), 1.16- 1.21 (6H, m); LCMS: 99.3%, MS (ESI): 596.2 m/z [M + H]+
81		off-white powder; 1H NMR (400 MHz, CD3OD): δ 8.56 (1H, s), 8.44 (1H, d, J = 6.8 Hz), 8.24 (1H, d. J = 6.4 Hz), 7.92-8.00 (1H, m), 7.81-7.91 (2H, m), 7.73 (1H, t, J = 7.2 Hz), 7.62 (1H, d, J = 7.6 Hz), 7.52-7.56 (1H, m), 7.46 (1H, s), 5.85 (1H, dd, J = 46.4, 4.0 Hz), 5.48 (1H, dd, J = 15.2, 4.0 Hz), 4.90-5.02 (2H, m), 4.73-4.83 (1H, m), 3.41 (3H, s), 3.23-3.32 (2H, m), 2.85-2.94 (1H, m), 1.99-2.24 (3H, m), 1.65-1.76 (1H, m), 1.30-1.55 (4H, m), 1.15-1.24 (6H, m); HPLC: 98.5% MS (ESI): m/z 608.2 [M + H]+
82		(3R, 4R); light yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.52-8.60 (1H, m), 8.44 (1H, J = 6.8 Hz), 8.22-8.26 (1H, m), 7.81-7.92 (3H, m), 7.67-7.72 (1H, m), 7.56-7.63 (2H, m), 7.48 (1H, s), 5.87 (1H, dd, J = 46.0, 2.8 Hz), 5.46 (1H, dd, J = 15.2, 4.0 Hz), 5.07-5.12 (1H, m), 4.73-4.79 (1H, m), 3.69-3.75 (1H, m), 3.37-3.56 (4H, m), 2.99-3.12 (1H, m), 2.81-2.97 (1H, m), 2.06-2.12 (1H, m), 1.82-1.89 (1H, m), 1.64-1.73 (1H, m), 1.17-1.24 (6H, m); LCMS: 99.7%; MS (ESI): 609.2 m/z [(M + H)]+
83		Mixture of 2 trans isomer; Yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.60-8.67 (1H, m), 8.48-8.52 (1H, m), 8.24- 8.28 (1H, m), 7.81-7.93 (3H, m), 7.56-7.73 (4H, m), 5.85 (1H, dd, J = 46.0, 3.6 Hz), 5.44 (1H, dd, J = 14.8. 3.6 Hz), 5.09-5.22 (1H, m), 4.67-4.77 (1H, m), 4.36-4.35 (1H, m), 3.46-3.62 (3H, m), 3.10-3.21 (2H, m), 2.81-2.88 (1H, m), 2.41-2.62 (1H, m), 1.16-1.22 (6H, m); LCMS: 100%, MS (ESI): 596.2 m/z [M + H]+
84		Yellow solid: 1H-NMR (CD3OD, 400 MHz): δ 8.63 (1H, s), 8.43 (1H, d, J = 6.8 Hz), 8.29 (1H, d, J = 6.8 Hz), 7.82-7.92 (3H, m), 7.65-7.71 (1H, m), 7.57-7.62 (2H, m), 7.54 (1H, s), 5.85 (1H. dd, J = 46.4, 3.6 Hz), 5.45 (1H, dd, J = 14.8, 3.6 Hz), 4.92-4.99 (1H, m), 4.72-4.80 (1H, m), 3.51-3.58 (1H, m), 3.39 (3H, s), 3.22-3.31 (1H, m, overlap with CD3OD signal), 2.76-2.83 (1H, m), 2.01-2.18 (3H, m), 1.69-1.73 (1H, m), 1.27-1.46 (4H, m), 1.15-1.21 (6H, m); LCMS: 100%, MS (ESI): 609.2 m/z [M + H]+
85		White powder; H NMR (CDCl3, 400 MHz): δ 8.54 (1H, d, J = 5.6 Hz), 8.30 (1H, s), 8.04 (1H, brs), 7.59 (1H, d, J = 8.8 Hz), 7.55 (2H, d, J = 6.0 Hz), 7.44 (1H, s), 7.30-7.42 (3H, m), 7.25 (1H, d, J = 8.8 Hz), 6.92-6.96 (1H, m), 5.85 (1H, dd, J = 47.6, 3.6 Hz), 5.26 (1H. dd, J = 14.8, 3.6 Hz), 4.76-4.85 (1H, m), 4.12-4.31 (3H, m), 3.42-3.53 (3H, m), 3.09-3.18 (2H, m), 2.83-2.96 (1H, m), 1.80-1.87 (2H, m), 1.43-1.51 (2H, m, overlap with water signal), 1.15-1.21 (9H, m); LCMS: 98.8%, MS (ESI): m/z 609.3 [M + H]+
86		Off-white powder; 1H NMR (CDCl3, 400 MHz): δ 8.62 (1H, d, J = 6.0 Hz), 8.41 (1H, s), 8.06-8.15 (1H, m), 7.61-7.75 (3H, m), 7.31-7.57 (5H, m), 7.02-7.23 (1H, m), 5.95 (1H, dd, J = 47.6, 3.2 Hz), 5.37 (1H, dd, J = 14.8, 3.2 Hz), 4.85-4.96 (1H, m), 4.46-4.54 (1H, m), 4.07-4.36 (2H, m), 3.47-3.60 (2H, m), 29.5-3.04 (1H, m), 1.92-2.05 (2H, m), 1.68-1.80 (2H, m), 1.27 (6H, d, J = 6.8 Hz); LCMS: 97.3%, MS (ESI): 649.1 m/z [M + H]+
87		Racemic mixture; off-white powder; 1H NMR (400 MHz, CD3OD) δ 8.39 (1H, s), 7.97 (1H, d, J = 6.4 Hz), 7.83-7.92 (2H, m), 7.73-7.80 (4H, m), 7.61-7.72 (3H, m), 7.56 (1H, d, J = 7.6 Hz), 7.44 (1H, t, J = 8.0 Hz), 7.12-7.16 (1H, m), 5.85 (1H, dd, J = 40.0, 4.0 Hz), 5.79 (1H, dd, J = 14.8, 3.6 Hz), 5.35-5.38 (1H, m), 5.03-5.07 (1H, m), 3.64-3.69 (1H, m), 3.18-3.27 (2H, m), 3.11-3.17 (1H, m), 2.41-2.48 (2H, m), 2.02-2.08 (1H, m), 1.58-1.64 (1H, m), 1.28-1.34 (6H, m); HPLC: 96.9% MS (ESI): m/z 643.2 [M + H]+
88		Yellow powder; 1H NMR (CDCl3, 400 MHz): δ 8.47 (1H, d, J = 6.0 Hz), 8.28 (1H, d, J = 1.2 Hz), 8.04-8.08 (1H, m), 7.59 (1H, d, J = 9.2 Hz), 7.52-7.57 (2H, m), 7.35-7.46 (3H, m), 7.26-7.34 (2H, m), 5.85 (1H, dd, J = 47.6, 3.6 Hz), 5.27 (1H, dd, J = 15.2, 3.6 Hz), 4.78-4.85 (1H, m), 4.08-4.24 (3H, m), 3.32-3.39 (4H, m), 3.19-3.30 (2H, m), 2.85-2.96 (1H, m), 1.79-1.84 (2H, m), 1.45-1.58 (2H, in, overlap with water signal), 1.17 (6H, d, J = 6.8 Hz); LCMS: 98%, MS (ESI): m/z 595.2 [M + H]+
89		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.62 (1H, d, J = 2.0 Hz), 8.42 (1H, d, J = 7.6 Hz), 8.21 (1H, d, J = 6.4 Hz), 7.79-7.91 (3H, m), 7.56-7.74 (4H, m), 5.94 (1H, dd, J = 46.4, 3.6 Hz), 5.48 (1H, dd, J = 14.8, 3.6 Hz), 4.94-5.02 (1H, m), 4.67-4.75 (1H, m), 3.91-4.02 (2H, m), 3.74-3.88 (2H, m), 3.46-3.59 (2H, m), 2.98-3.07 (1H, m), 1.82-1.93 (2H, m), 1.47-1.65 (2H, m), 1.18-1.23 (12H, m); LCMS: 99.9%, MS (ESI): 623.2 m/z [M + H]+
90		White solid: 1H NMR (CDCl3 400 MHz,) δ 8.62 (1H, d, J = 5.6 Hz), 8.38 (1H, d, J = 2.0 Hz), 8.16-8.21 (1H, m), 7.69 (1H, d, J = 8.8 Hz), 7.60-7.65 (2H, m), 7.54 (1H, s), 7.43-7.49 (3H, m), 7.39-7.42 (1H, m), 7.09-7.16 (1H, m), 5.91 (1H, dd, J = 47.6, 3.6 Hz), 5.35 (1H, dd, J = 15.2, 3.6 Hz), 4.76-4.95 (2H, m), 4.18-4.29 (1H, m), 3.71-3.92 (4H, m), 2.93-3.05 (1H, m), 1.78-1.94 (4H, m), 1.26 (6H, d, J = 6.8 Hz); LCMS: 100.0%, MS (ESI): m/z 583.1 [M + H]+.
91		Yellow powder; 1H-NMR (CD3OD, 400 MHz): δ 8.41 (1H, d, J = 5.6 Hz), 8.36 (1H, d, J = 1.6 Hz), 7.66-7.72 (2H, m), 7.54-7.59 (1H, m), 7.46-7.52 (2H, m), 7.35-7.42 (3H, m), 5.78 (1H, dd, J = 46.4, 3.6 Hz), 5.36 (1H, dd, J = 14.8, 3.2 Hz), 5.02 (1H. s), 4.48-4.55 (1H, m), 4.35-4.41 (1H, m), 3.80-3.95 (2H, m), 3.42-3.48 (1H, m), 3.38 (3H, s), 3.04- 3.15 (2H, m), 2.91-2.98 (1H, m), 1.86-1.92 (2H, m), 1.38- 1.51 (2H, m), 1.22 (6H, d, J = 6.8 Hz); LCMS: 98.5%, MS (ESI): 594.2 m/z [(M + H)]+.
92		White powder; 1H NMR (CDCl3, 400 MHz): δ 8.60 (1H, brs), 8.38-8.41 (1H, m), 8.23 (1H, brs), 7.72 (1H. d, J = 9.2 Hz), 7.58-7.63 (2H, m), 7.56 (1H, s), 7.38-7.51 (4H, m), 5.90 (1H, dd, J = 47.6, 3.6 Hz), 5.84 (1H, d, J = 15.2, 3.2 Hz), 4.73-4.89 (2H, m), 4.48-4.55 (1H, m), 4.19-4.28 (1H, m), 3.91-4.03 (2H, m), 3.83-3.89 (1H, m), 3.66-3.71 (1H, m), 2.92-3.03 (1H, m), 2.23-2.31 (1H, m), 1.79-1.87 (1H, m), 1.22-1.29 (7H, m); LCMS: 97.4%, MS (ESI): m/z 567.2 [M + H]+
93		White solid; 1H-NMR (CDCl3, 400 MHz): δ 10.59 (1H, brs), 8.82-8.84 (1H, m), 8.18 (1H, d, J = 8.8 Hz), 7.56-7.61 (3H, m), 7.50 (1H, s), 7.35-7.40 (3H, m), 6.24 (1H, t, J = 4.8 Hz), 5.82 (1H, dd, J = 46.8, 3.2 Hz), 5.21 (1H, dd, J = 14.8, 3.2 Hz), 4.83-4.87 (2H, m), 4.14-4.19 (2H, m), 3.35- 3.40 (4H, m), 3.14-3.21 (2H, m), 2.96-2.99 (1H, m), 2.55 (3H, s), 1.82-1.85 (2H, m), 1.41-1.49 (2H, m), 1.26 (6H, d, J = 6.8 Hz); LCMS: 100.0%, MS (ESI): 609.2 m/z [(M + H)]+.
94		off-white powder; 1H NMR (400 MHz, CD3OD) δ 8.53- 8.62 (1H, m), 8.41-8.45 (1H, m), 8.22 (1H, d, J = 6.4 Hz), 7.79-7.97 (3H, m), 7.68-7.74 (1H, m), 7.56-7.66 (2H, m), 7.50 (1H, d, J = 7.6 Hz), 5.79-5.97 (1H, m), 5.46 (1H, dd, J = 14.8, 3.6 Hz), 4.93-5.00 (2H, m, overlap with water signal), 3.96-4.17 (2H, m), 3.81- 3.88 (1H, m), 3.52-3.64 (1H, m), 3.41-3.51 (2H, m), 2.84-3.24 (4H, m), 1.10-1.29 (6H, m); HPLC: 96.4% MS (ESI): m/z 595.2 [M + H]+.
95		White solid; 1H-NMR (CDCl3, 400 MHz): δ 8.58 (1H, d, J = 5.6 Hz), 8.41-8.48 (1H, m), 7.77 (1H, brs), 7.53-7.68 (4H, m), 7.39-7.48 (3H, m), 7.30-7.34 (1H, m), 7.23 (1H, brs), 6.52 (1H, dd, J = 12.6, 1.2 Hz), 6.31 (1H, dd, J = 16.8, 10.0 Hz), 5.85 (1H, dd, J = 10.0, 1.2 Hz), 4.79-4.91 (1H m), 4.14-4.22 (1H, m), 3.68-3.75 (1H, m), 3.38 (3H, s), 3.14-3.22 (1H, m), 2.92-3.02 (1H, m), 1.81-2.13 (5H, m, overlap with water signal), 1.15-1.38 (9H, m).; LCMS: 100%, MS (ESI): 591.2 m/z [M + H]+.
96		Cis or trans form; yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.64-8.67 (1H, m), 8.43-8.51 (1H, m), 8.23-8.29 (1H, m), 7.78-7.93 (3H, m), 7.56-7.74 (4H, m), 5.88 (1H, dd, J = 46.0, 2.0 Hz), 5.48 (1H, dd. J = 15.2, 4.0 Hz), 4.97- 5.09 (1H, m), 4.66-4.76 (1H, m), 4.16-4.25 (1H, m), 3.93- 4.02 (1H, m), 3.39 (3H, s), 2.77-2.84 (1H, m), 1.63-2.16 (5H, m), 1.53-1.62 (1H, m), 1.18-1.26 (6H, m); LCMS: 97.9%, MS (ESI): 595.2 m/z [M + H]+
97		Cis or trans form; yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.64-8.67 (1H, m), 8.43-8.51 (1H, m), 8.23-8.29 (1H, m), 7.78-7.93 (3H, m), 7.56-7.74 (4H, m), 5.88 (1H, dd, J = 46.0, 2.0 Hz), 5.48 (1H, dd, J = 15.2, 4.0 Hz), 4.97- 5.09 (1H, m), 4.66-4.76 (1H, m), 4.16-4.25 (1H, m), 3.93- 4.02 (1H, m), 3.39 (3H, s), 2.77-2.84 (1H, m), 1.63-2.16 (5H, m), 1.53-1.62 (1H, m), 1.18-1.26 (6H, m); LCMS: 99.8%, MS (ESI): 595.2 m/z [M + H]+
98		Racemic mixture; yellow powder; yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.64-8.67 (1H, m), 8.43-8.51 (1H, m), 8.23-8.29 (1H, m), 7.78-7.93 (3H, m), 7.56-7.74 (4H, m), 5.88 (1H, dd, J = 46.0, 2.0 Hz), 5.48 (1H, dd, J = 15.2, 4.0 Hz), 4.97-5.09 (1H, m), 4.66-4.76 (1H, m), 4.16-4.25 (1H, m), 3.93-4.02 (1H, m), 3.39 (3H, s), 2.77-2.84 (1H, m), 1.63-2.16 (5H, m), 1.53-1.62 (1H, m), 1.18-1.26 (6H, m); LCMS: 99.8%, MS (ESI): 595.2 m/z [M + H]+
99		White solid; 1H NMR (CD3OD, 400 MHz,) δ 8.58-8.64 (1H, m), 8.39-8.42 (1H, m), 8.10-8.18 (1H, m), 7.78-7.85 (3H, m), 7.61-7.69 (2H, m), 7.56-7.60 (2H, m), 5.85 (1H, dd, J = 46.0, 3.2 Hz), 5.45 (1H, dd, J = 14.8, 3.2 Hz), 4.98- 5.05 (1H, m), 4.63-4.75 (1H, m), 3.67-3.78 (2H, m), 3.28 (3H, s), 2.76-2.84 (2H, m), 2.53-2.61 (1H, m), 1.83-2.02 (2H, m), 1.17-1.22 (6H, m); LCMS: 100.0%, MS (ESI): m/z 581.2 [M + H]+.
100		Yellow solid; 1H NMR (CDCl3, 400 MHz) δ 8.56-8.61 (1H, m), 8.44-8.53 (1H, m), 8.22-8.27 (1H, m), 7.92-7.97 (1H, m), 7.81-7.85 (2H, m), 7.54-7.71 (4H, m), 5.87 (1H. dd, J = 46.0, 3.6 Hz), 5.46 (1H, dd, J = 15.2, 3.6 Hz), 3.42-3.96 (7H, m), 3.34 (3H, s), 3.03-3.15 (1H, m), 1.47-2.13 (5H, m), 1.20-1.24 (1H, m), 1.14-1.22 (6H, m); LCMS: 99.2%, MS (ESI): m/z 609.2 [M + H]+
101		Yellow powder: 1H NMR (CD3OD, 400 MHz): δ 8.55 (1H, d, J = 2.0 Hz), 8.03-8.12 (1H, m), 7.97 (1H, d, J = 6.4 Hz), 7.82-7.85 (2H, m), 7.63-7.67 (2H, m), 7.50-7.54 (3H, m), 7.29 (1H, d, J = 5.2 Hz), 6.93-7.02 (1H, m), 6.88 (1H, d, J = 4.8 Hz), 6.62 (1H, d, J = 15.2 Hz), 4.68-4.75 (1H, m), 4.01-4.09 (3H, m), 3.89-3.97 (1H, m), 3.56-3.61 (1H, m), 3.43-3.48 (1H, m), 2.91-3.02 (9H, m), 1.17-1.22 (6H, m).; LCMS: 100%, MS (ESI): m/z 658.2 [M + H]+
102		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.67 (1H, d, J = 1.6 Hz), 8.33-8.42 (1H, m), 8.18-8.25 (1H, m), 7.80- 7.91 (3H, m), 7.67-7.72 (1H, m), 7.57-7.65 (3H, m), 6.99- 7.10 (1H, m), 6.76 (1H, d, J = 15.6 Hz), 4.73-4.84 (2H, m), 4.40-4.55 (2H, m), 4.09 (2H, d, J = 6.8 Hz), 3.97-4.06 (2H, m), 3.35-3.38 (2H, m, overlap with CD3OD signal), 3.05- 3.19 (1H, m), 2.98 (6H, s), 1.47-2.14 (4 H, m), 1.14-1.26 (6H, m); HPLC (254 nm): 100% MS (ESI): m/z 632.2 [M + H]+
103		off-white powder; 1H NMR (CD3OD, 400 MHz): δ 8.62 (1H, s), 8.27-8.46 (1H, m), 8.11-8.18 (1H, m), 7.70-7.88 (3H, m), 7.63-7.69 (1H, m), 7.50-7.58 (3H, m), 6.96-7.07 (1H, m), 6.72 (1H, d, J = 15.2 Hz), 4.87-4.92 (2H, m, overlap with water signal), 4.63-4.72 (1H, m), 4.07 (2H, d, J = 6.8 Hz), 3.46-3.49 (1H, m), 3.30-3.33 (4H, m), 3.01- 3.12 (1H, m), 2.96 (6H, s), 1.51-2.43 (8H, m), 1.17 (6H, d, J = 6.4 Hz); LCMS: 100%, MS (ESI): m/z 660.3 [M + H]+
104		Yellow solid; 1H NMR (CD3OD, 400 MHz): δ 8.62-8.66 (1H, m), 8.40 (1H, d, J = 6.4 Hz), 8.21 (1H, d, J = 6.4 Hz), 7.81-7.88 (3H, m), 7.68-7.72 (2H, m), 7.58-7.61 (2H, m), 6.99-7.07 (1H, m), 6.75 (1H, d, J = 14.8 Hz), 4.80-4.84 (1H, m, overlap with water signal), 4.72-4.75 (1H, m), 4.07 (2H, d, J = 6.8 Hz), 3.66-3.88 (9H, m), 3.08-3.15 (2H, m), 2.96 (6H, s), 1.16-1.21 (6H, m); LCMS: 100.0%, MS (ESI): 632.2 m/z [M + H]+
105		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.29-8.33 (2H, m), 7.64-7.68 (1H, m), 7.57-7.62 (2H, m), 7.51-7.55 (1H, m), 7.32-7.43 (4H, m), 6.96-7.02 (1H, m), 6.32 (1H, d, J = 15.6 Hz), 4.92-4.95 (1H, m, overlap with water signal), 4.36-4.43 (1H, m), 3.86-3.94 (2H, m), 3.38-3.47 (2H, m), 3.23 (2H, d, J = 6.8 Hz), 2.96-3.03 (1H, m), 2.83-2.90 (1H, m), 2.34 (6H, s), 1.80-1.92 (2H, m), 1.64-1.78 (2H, m), 1.17-1.23 (6H, m); LCMS: 99.2%, MS (ESI): 629.2 m/z [M + H]+
106		off-white solid; 1H NMR (CD3OD, 400 MHz) δ 8.58 (1H, s), 8.21-8.28 (1H, m), 7.99-8.04 (1H, m), 7.77-7.81 (2H, m), 7.62-7.73 (2H, m), 7.52-7.59 (2H, m), 7.41-7.45 (1H, m), 6.97-7.06 (1H, m), 6.63-6.72 (1H, m), 4.67-4.73 (2H, m), 4.07 (2H, d, J = 6.8 Hz), 3.54-3.70 (4H, m), 2.96 (6H, s), 1.93-2.16 (2H, m), 1.63-1.78 (2H, m), 1.21-1.28 (6H, m); LCMS: 100.0%, MS (ESI): m/z 618.2 [M + H]+
107		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.30-8.35 (2H, m), 7.63-7.66 (1H, m), 7.55-7.62 (2H, m), 7.48-7.53 (1H, m), 7.40-7.45 (2H, m), 7.32-7.38 (2H, m), 6.91-7.01 (1H, m), 6.39 (1H, d, J = 15.6 Hz), 4.95-4.98 (1H, m, overlap with water signal), 4.30-4.37 (1H, m), 3.88-3.95 (1H, m), 3.44 (2H, d, J = 6.4 Hz), 3.18-3.24 (2H, m), 3.08- 3.16 (2H, m), 2.1-2.90 (1H, m), 2.50 (6H, s), 2.26-2.35 (2H, m), 2.01-2.20 (2H, m), 1.16-1.22 (6H, m); LCMS: 100%, MS (ESI): m/z 668.3 [M + H]+
108		white solid; 1H NMR (CD3OD, 400 MHz) δ 8.30 (1H, d, J = 1.6 Hz), 8.26 (1H, d, J = 6.0 Hz), 7.63-7.66 (1H, m), 7.55-7.60 (2H, m), 7.48-7.53 (1H, m), 7.31-7.47 (4H, m), 6.91-7.02 (1H, m), 6.33 (1H, d, J = 15.6 Hz), 4.86- 4.90 (1H, m, overlap with water signal), 4.79-4.84 (4H, m), 4.35-4.41 (1H, m), 3.95-4.07 (4H, m), 3.28 (2H, d, J = 6.4 Hz), 2.88-2.97 (1H, m), 2.37 (6H, s), 1.16-1.21 (6H, m); LCMS: 100.0%, MS (ESI): m/z 618.1 [M + H]+
109		Yellow solid; 1H-NMR (CD3OD, 400 MHz): δ 8.65-8.68 (1H, m), 8.42-8.47 (1H, m), 8.18-8.21 (1H, m), 7.80-7.87 (3H, m), 7.67-7.73 (2H, m), 7.56-7.62 (2H, m), 6.98-7.05 (1H, m), 6.68-6.75 (1H, m), 5.03-5.18 (1H, m), 4.72-4.78 (1H, m), 4.28-4.36 (1H, m), 4.06 (2H, d, J = 7.2 Hz), 3.31- 3.62 (4H, m), 3.12-3.23 (2H, m), 2.95 (6H, s), 2.83-2.92 (1H, m), 2.38-2.61 (1H, m), 1.18-1.22 (6H, m); LCMS: 100%, MS (ESI): 635.2 m/z [M + H]+
110		White solid: 1H NMR (CD3OD, 400 MHz) δ 8.28-8.32 (2H, m), 7.64-7.67 (1H, m), 7.54-7.61 (2H, m) 7.46-7.52 (1H, m), 7.31-7.39 (4H, m), 6.91-6.99 (1H, m), 6.37 (1H, d, J = 15.2 Hz), 4.79-4.84 (1H, m, overlap with water signal), 4.36-4.41 (1H, m), 3.98 (4H, s), 3.60-3.74 (4H, m), 3.37- 3.43 (2H, m), 2.81-2.91 (1H, m), 2.44-2.52 (6H, m), 1.52- 1.64 (4H, m), 1.19 (6H, d, J = 5.6 Hz); LCMS: 100.0%, MS (ESI): m/z 662.3 [M + H]+
111		Yellow solid; 1H NMR (CD3OD, 400 MHz): δ 8.58-8.64 (1H, m), 8.40-8.46 (1H, m), 8.19 (1H, d, J = 6.8 Hz), 7.63- 7.89 (5H, m), 7.55-7.62 (2H, m), 6.48-6.52 (2H, m), 5.89- 5.94 (1H, m), 5.06-5.23 (1H, m), 4.66-4.76 (1H, m), 4.26- 4.36 (1H, m), 3.34-3.61 (4H, m), 3.12-3.21 (2H, m), 2.78- 2.85 (1H, m), 2.38-2.61 (1H, m), 1.15-1.21 (6H, m); LCMS: 100%, MS (ESI): 578.2 m/z [M + H]+
112		White solid; 1H NMR (CDCl3, 400 MHz): δ 9.77 (1H, s), 8.88 (1H, dd, J = 6.0, 2.8 Hz), 8.23 (1H, d, J = 8.4 Hz), 7.55-7.61 (4H, m), 7.34-7.43 (3H, m), 6.62 (1H, brs), 6.30- 6.44 (2H, m), 5.58 (1H, dd, J = 9.2, 2.0 Hz), 4.68 (2H, d, J = 5.2 Hz), 4.58-4.63 (1H, m), 3.73-3.76 (1H, m), 3.35 (3H, s), 3.12-3.18 (1H, m), 2.96-3.03 (1H, m), 2.53 (3H, s), 2.03-2.13 (4H, m), 1.13-1.35 (10H, m); LCMS: 98.7%, MS (ESI): 606.3 m/z [(M + H)]+
113		White solid; 1H NMR (CDCl3, 400 MHz) δ 8.56 (1H, d, J = 5.6 Hz), 8.39 (1H, d, J = 1.6 Hz), 7.68 (1H, d, J = 8.8 Hz), 7.60-7.63 (2H, m), 7.55-7.59 (1H, m), 7.45-7.49 (3H, m), 7.41-7.45 (1H, m), 7.37 (1H, dd, J = 8.8, 2.0 Hz), 6.54 (1H, dd, J = 16.8, 1.2 Hz), 6.30 (1H, dd, J = 16.8, 10.4 Hz), 5.88 (1H, dd, J = 10.4, 1.2 Hz), 4.74-4.85 (1H, m), 4.24-4.36 (5H, m), 2.93-3.05 (5H, m), 1.27 (6 H, d, J = 6.8 Hz); LCMS: 100.0%, MS (ESI): m/z 597.1 [M + H]+
114		Light yellow powder: 1H NMR (CDCl3, 400 MHz): δ 8.61 (1H, d, J = 5.6 Hz), 8.40 (1H, brs), 7.62-7.70 (3H, m), 7.53- 7.57 (2H, m), 7.38-7.49 (3H, m), 7.28-7.35 (1H, m), 6.53 (1H, d, J = 16.8 Hz), 6.27-6.35 (1H, m), 5.87 (1H, d, J = 10.4 Hz), 4.80-4.86 (1H, m), 4.55-4.64 (2H, m), 4.21-4.27 (1H, m), 4.02-4.11 (1H, m), 2.95-3.04 (1H, m), 2.15-2.26 (3H, m), 1.98-2.06 (2H, m), 1.71-1.75 (2H, m), 1.50-1.55 (1H, m), 1.26 (6H, d, J = 7.2 Hz); LCMS: 100.0%, MS (ESI): 589.1 m/z [(M + H)]+
115		Light yellow solid; 1H NMR (CD3OD, 400 MHz): δ 8.28- 8.31 (2H, m), 7.43-7.65 (4H, m), 7.28-7.39 (4H, m), 6.92- 7.00 (1H, m), 6.31 (1H, d, J = 15.2 Hz), 4.73-4.80 (1H, m, overlap with water signal), 4.36-4.42 (1H, m), 3.89 (4H, s), 3.49-3.82 (4H, m), 3.23 (2H, d, J = 6.8 Hz), 2.78-2.87 (1H, m), 2.33 (6H, s), 1.56-1.91 (6H, m), 1.15-1.20 (6H, m); LCMS: 99.0%, MS (ESI): 676.2 m/z [M + H]+
116		White powder; 1H NMR (CDCl3, 400 MHz): δ 8.49 (1H, d, J = 5.6 Hz), 8.38 (1H. brs), 7.55-7.65 (2H, m), 7.43-7.52 (3H, m), 7.29-7.42 (3H, m), 7.14-7.18 (1H, m, overlap with CDCl3 signal), 6.45 (1H, d, J = 16.8 Hz), 6.17-6.28 (2H, m), 5.78 (1H, d, J = 7.2 Hz), 4.71 (1H, s), 4.12-4.35 (2H, m), 3.21-3.50 (4H, m), 3.03-3.16 (1H, m), 2.89-2.97 (1H, m), 1.79-2.12 (4H, m), 1.02-1.33 (10H, m): LCMS: 99.9%, MS (ES1): 590.2 m/z [M + H]+
117		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.65 (1H, d, J = 1.60 Hz), 8.35 (1H, d, J = 6.80 Hz), 8.15 (1H, d, J = 6.40 Hz), 7.79-7.88 (3H, m), 7.56-7.73 (4H, m), 6.97-7.12 (1H, m), 6.75 (1H, d, J = 15.20 Hz), 4.75 (2H, br d, J = 15.60 Hz), 4.09 (2H, d, J = 7.00 Hz), 3.93 (2H, t, J = 7.20 Hz) 3.60-3.78 (6H, m), 3.03-3.10 (1H, m), 2.98 (6H, s), 1.90 (2H, t, J = 7.20 Hz), 1.65 (4H, br s), 1.21 (6H, dd, J = 6.80, 5.60 Hz); HPLC: 100% MS (ESI): m/z 660.2 [M + H]+
118		White powder; 1H NMR (400 MHz, CD3OD) δ 8.56 (1H, d, J = 5.60 Hz), 8.42 (1H, s), 7.36-7.68 (7H, m), 6.53 (1H, d, J = 17.20 Hz), 6.24-6.38 (2H, m), 5.87 (1H, d, J = 10.40 Hz), 5.16 (1H, s), 4.35 (2H, d, J = 5.60 Hz), 4.01 (4H. s), 3.62-3.74 (4H, m), 2.99-3.12 (1H, m), 1.68-1.79 (4H, m), 1.30 (6H, d, J = 7.00 Hz); HPLC: 97.2% MS (ESI): m/z 604.1 [M + H]+
119		White powder; 1H NMR (CDCl3, 400 MHz): δ 8.56 (1H, d, J = 5.6 Hz), 8.43 (1H, s), 7.36-7.65 (8H, m), 7.20 (1H, dd, J = 2.0 and 9.1 Hz), 6.52 (1H, d, J = 16.8 Hz), 6.24-6.34 (2H, m), 5.86 (1H, d, J = 10.5 Hz), 5.00 (1H, s), 4.22-4.42 (4H, m), 3.72 (1H, br d, J = 3.6 Hz), 3.34 (1H, br s), 3.28 (3H, s), 3.02 (1H, quin, J = 6.8 Hz), 2.10 (2H, br d, J = 7.1 Hz), 1.91-2.05 (3H, m), 1.66-1.91 (3H, m), 1.27 (6H, d, J = 6.9 Hz); LCMS: 100%, MS (ESI): m/z 602.5 [M + H]+
120		Yellow solid; 1H NMR (CD3OD, 400 MHz): δ 8.61 (1H, d, J = 2.0 Hz), 8.34 (1H, d, J = 6.8 Hz), 8.12 (1H, d, J = 6.8 Hz), 7.64-7.86 (4H, m), 7.53-7.60 (2H, m), 7.47 (1H, s), 6.97-7.06 (1H, m), 6.71 (1H, d, J = 15.2 Hz), 4.95-5.01 (1H, m), 4.68-4.74 (1H, m), 4.06 (2H, d, J = 7.2 Hz), 3.46- 3.81 (6H, m), 3.34-3.40 (2H, m), 3.14-3.25 (2H, m), 2.93- 3.02 (7H, m), 2.87 (3H, s), 2.09-2.21 (2H, m), 1.79-1.92 (2H, m), 1.14-1.19 (6H, m); LCMS: 98.6%, MS (ESI): 689.4 m/z [M + H]+
121		Pale yellow solid; 1H NMR (400 MHz, CD3OD) δ 8.61 (1H, s), 8.39 (1H, d, J = 6.4 Hz), 8.17 (1H, d, J = 6.4 Hz), 7.79-7.81 (3H, m), 7.64-7.67 (1H, m), 7.54-7.63 (3H, m), 6.99-7.05 (1H, m), 6.76 (1H, d, J = 14.8 Hz), 4.95-4.99 (1H, m), 4.68-4.71 (1H, m), 4.08 (2H, d, J = 7.2 Hz), 3.76-3.81 (3H, m), 3.67-3.73 (3H, m), 3.02- 3.06 (2H, m), 2.99 (3H, s), 2.96 (6H, s), 2.17-2.20 (1H, m), 2.06-2.11 (1H, m), 1.72-1.77 (4H, m), 1.19 (6H, d, J = 6.8 Hz); LCMS: 99.8%, MS (ESI): 673.4 m/z [M + H]+
122		Yellow powder; 1H NMR (CD3OD, 400 MHz) δ 8.64 (1H, d, J = 2 Hz), 8.36 (1H, d, J = 6.8 Hz), 8.14 (1H, d, J = 6.4 Hz), 7.77-7.86 (2H, m), 7.69-7.75 (1H, m), 7.61-7.69 (2H, m), 7.58 (1H, s), 7.55 (1H, d, J = 7.6 Hz), 6.97-7.08 (1H, m), 6.70 (1H, d, J = 14.8 Hz), 5.09 (1H, m), 5.01 (1H, d, J = 15.6 Hz), 4.64 (1H, d, J = 15.6 Hz), 4.07 (2H, d, J = 7.6 Hz), 3.93 (2H, m), 2.96 (6H, s), 2.89 (1H, m), 2.83 (3H, s), 2.03-2.58 (8H, m), 1.21 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 660.5 [M + H]+
123		White solid: 1H NMR (CD3OD 400 MHz) δ 8.54 (1H, s), 8.32 (1H, d, J = 6.8 Hz), 8.09 (1H, d, J = 6.8 Hz), 7.77-7.82 (2H, m), 7.61-7.64 (2H, m), 7.49-7.53 (2H, m), 7.33 (1H, s), 6.97-7.03 (1H, m), 6.71 (1H, d, J = 15.2 Hz), 4.95-5.00 (2H, m), 4.39-4.68 (2H, m), 4.00-4.08 (4H, m), 3.31-3.44 (1H, m), 2.96 (6H, s), 2.86 (3H, s), 2.81-2.86 (1H, m), 2.21-2.26 (2H, m), 1.88-1.93 (1H, m), 1.67-1.72 (2H, m), 1.27- 1.32 (2H, m), 1.18 (6H, d, J = 6.8 Hz); LCMS: 99.5%, MS (ESI): m/z 645.4 [M + H]+
124		White powder; 1H NMR (400 MHz, CD3OD) δ 8.32-8.47 (2H, m), 7.68-7.74 (2H, m), 7.56-7.62 (1 H, m), 7.52 (1H, t, J = 7.60 Hz), 7.34-7.41 (4H, m), 6.99 (1H, dt, J = 15.37, 6.49 Hz), 6.34 (1H, d, J = 15.60 Hz), 5.03 (1H, s), 4.55 (1H, br d, J = 15.56 Hz), 4.37-4.45 (1H, m), 4.00 (4H, s), 3.50-3.71 (4H, m), 3.24 (2H, d, J = 5.60 Hz), 2.91-2.99 (1H, m), 2.34 (6H, s), 1.56-1.71 (4H, m), 1.23 (6H, d, J = 8.00 Hz); HPLC: 99.4% MS (ESI): m/z 661.3 [M + H]+
125		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.57 (1H, d, J = 1.8 Hz), 8.37 (1H, d, J = 6.5 Hz), 8.07 (1H, d, J = 6.3 Hz), 7.84-7.90 (1H, m), 7.80 (1H, t, J = 7.2 Hz), 7.64- 7.74 (2H, m), 7.49-7.58 (3H, m), 6.94-7.07 (1H, m), 6.73 (1H, d, J = 15.3 Hz), 4.99 (1H, s), 4.94 (1H, br s), 4.65- 4.75 (1H, m), 4.49 (2H, br s), 4.06 (2H, d, J = 7.3 Hz), 3.46-3.52 (1H, m), 3.33 (3H, s), 3.11-3.21 (1H, m), 2.96 (6H, s), 2.30 (2H, br d, J = 7.5 Hz), 1.92-2.11 (5H, m), 1.68 (1H, br s), 1.18 (6H, dd, J = 6.9 and 12.2 Hz).. LCMS: 98.2%, MS (ESI): m/z 659.5 [M + H]+
126		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.65 (1H, s), 8.35-8.47 (1H, m), 8.22 (1H, d, J = 6.40 Hz), 7.78-7.92 (3H, m), 7.53-7.73 (4H, m), 6.94-7.11 (1H, m), 6.74 (1H, d, J = 14.40 Hz), 4.95-5.02 (1H, m), 4.75-4.82 (1H, m), 4.34- 4.55 (2H, m), 4.07 (2H, d, J = 7.20 Hz), 3.51-3.63 (1H, m), 3.02-3.25 (3H, m), 2.96 (12H, s). 1.52-2.27 (4H, m), 1.18 (6H, t, J = 6.78 Hz): HPLC: 100%, MS (ESI): 711.5 m/z [M + H]+
127		White powder; 1H NMR (CD3OD, 400 MHz) δ 8.67 (1 H, d, J = 8.0 Hz) 8.29 (1 H, d, J = 8.4 Hz) 7.65 (2 H, d, J = 9.2 Hz) 7.53-7.59 (2 H, m) 7.40-7.44 (2 H, m) 7.34-7.39 (1 H, m) 6.78-6.91 (1 H, m) 6.27 (1 H, s) 4.76 (2 H, s) 3.33 (3 H, s) 3.14 (3 H, s) 2.92 (1 H, t, J = 8.4 Hz) 2.56 (3 H, s) 2.33 (6 H, s) 2.02 (4 H, d, J = 12.0 Hz) 1.29 (2 H, s) 1.24 (6 H, d, J = 6.8 Hz) 1.17 (2 H, s); LCMS: 92.5%, MS (ESI): m/z 662.5 [M + H]+
128		Yellow solid: 1H NMR (CD3OD, 400 MHz) δ 8.67 (1 H, d, J = 1.2 Hz) 8.44 (1 H, d, J = 6.4 Hz) 8.23 (1 H, d, J = 6.4 Hz) 7.88 (1 H, dd, J = 9.2, 1.6 Hz) 7.80-7.85 (2 H, m) 7.65-7.72 (2 H, m) 7.62 (1 H, s) 7.58-7.61 (1 H, m) 6.99- 7.09 (1 H, m) 6.76 (1 H, d, J = 15.56 Hz) 5.01 (2 H, br d, J = 15.6 Hz) 4.73 (1 H, d, J = 15.6 Hz) 4.08 (2 H, d. J = 6.8 Hz) 3.77 (4 H, s) 3.43 (2 H, d, J = 12.0 Hz) 3.19-3.24 (2 H, m) 3.08-3.16 (1 H, m) 2.96 (6 H, s) 2.92 (3 H, s) 1.93-2.13 (2 H, m) 1.84 (2 H, s) 1.71-1.78 (2 H, m) 1.54- 1.65 (2 H, m) 1.18 (6 H, dd. J = 6.8, 3.2 Hz); LCMS: 100.0%, MS (ESI): m/z 687.6 [M + H]+
129		White powder; 1H NMR (CD3OD, 400 MHz): δ 7.72 (1H, s), 7.37 (3H, s), 7.25-7.34 (2H, m), 6.98 (1H, t, J = 7.80 Hz), 6.81-6.92 (1H, m), 6.70-6.78 (1H, m), 6.35 (1H, s), 5.00 (2H, s), 4.01 (2H, d, J = 7.03 Hz), 3.59-3.76 (1H, m), 3.32-3.38 (3H, m), 3.12-3.20 (1H, m) 2.94 (7H, s), 2.55 (3H, s), 1.85-2.05 (4H, m), 1.22-1.31 (10H, m); HPLC: 98.0%, MS (ESI): 650.5 m/z [M + H]+
130		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.60-8.72 (1H, m), 8.41 (1H, d, J = 6.8 Hz), 8.20 (1H, d, J = 5.6 Hz), 7.78-7.89 (3H, m), 7.53-7.73 (4H, m), 6.96-7.10 (1H, m), 6.71 (1H, d, J = 15.2 Hz), 5.01 (2H, m), 4.72 (1H, d, J = 15.6 Hz), 4.07 (2H, d, J = 6.8 Hz), 3.90-3.99 (2H, m), 2.96 (6H, s), 2.81-2.90 (4H, m), 2.06-2.66 (8H, m), 1.23 (6H, m); LCMS: 100%, MS (ESI): m/z 659.4 [M + H]+
131		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.57 (1H, s), 8.41 (1H, s), 8.06 (1H, s), 7.50-7.88 (7 H, m), 6.92-7.08 (1H, m) 6.66 (1 H, d, J = 15.20 Hz), 4.96-5.19 (2H, m), 4.62-4.80 (1H, m), 4.06 (2 H, d, J = 7.20 Hz), 3.38-3.69 (7H, m), 2.81-3.03 (9H, m), 1.88-2.12 (2H, m), 1.58 (1H, s), 1.18 (6H, d, J = 6.80 Hz); HPLC: 99.8% MS (ESI): m/z 663.6 [M + H]+
132		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.55 (1H, s), 8.40 (1 H, d, J = 6.40 Hz), 8.03 (1H, s), 7.76-7.89 (2H, m), 7.59-7.70 (2H, m), 7.43-7.57 (3H, m), 6.96-7.03 (1H, m), 6.70 (1H, d, J = 15.20 Hz), 4.95-5.02 (2H, m) 4.65-4.75 (2H, m), 4.06 (2H, d, J = 7.20 Hz), 3.38 (3H, s) 3.21-3.28 (1 H, m), 2.91-3.01 (7H, m), 2.00-2.19 (3H, m), 1.72 (1H, s), 1.29-1.48 (4 H, m) 1.18 (6 H, dd, J = 14.00, 6.80 Hz); HPLC: 100% MS (ESI): m/z 647.4 [M + H]+
133		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.65 (1H, s), 8.43 (1H, d, J = 6.4 Hz), 8.18 (1H, d, J = 6.8 Hz), 7.76- 7.93 (3H, m), 7.54-7.74 (4H, m), 6.97-7.09 (1H, m), 6.72 (1H, d, J = 15.6 Hz), 5.05 (1H, d, J = 15.6 Hz), 4.70-4.79 (1 H, m), 4.07 (2H, d, J = 7.2 Hz), 3.53 (2H, d, J = 10.4 Hz), 3.10-3.27 (2H, m), 3.01 (2H, m), 2.96 (6H, s), 2.86 (4H, m), 1.80-2.10 (3H, m), 1.61 (2H, m), 1.16-1.25 (6H, m); LCMS: 100%, MS (ESI): m/z 647.4 [M + H]+
134		White powder; 1H NMR (CD3OD, 400 MHz) δ 8.68 (1H, s), 8.39 (1H, d, J = 6.8 Hz), 8.24 (1H, d, J = 6.8 Hz), 7.78-7.92 (3H, m), 7.68 (1H, m), 7.52-7.65 (3H, m), 7.02 (1H, m), 6.71 (1H, d, J = 14.8 Hz), 4.94-4.95 (1H, m), 4.81-4.82 (1H, m), 4.07 (2H, d, J = 7.2 Hz), 3.05 (2H, d, J = 5.2 Hz), 2.96 (6H, s), 2.77-2.91 (2H, m), 2.74 (3H, s), 1.70-2.16 (5H, m), 1.28-1.52 (4H, m), 1.13-1.22 (6H, m); LCMS: 100%, MS (ESI): m/z 725.4 [M + H]+
135		White powder; 1H NMR (CD3OD, 400 MHz): δ 8.47 (1H, s), 8.40 (1H, d, J = 6.4 Hz), 8.22 (1H, d, J = 6.4 Hz), 7.78-7.88 (2H, m), 7.63-7.72 (2H, m), 7.52-7.61 (3H, m), 4.97 (1H, s), 4.75 (1H, d, J = 16 Hz), 3.45-3.60 (1H, m), 3.40 (3H, s), 3.25 (1H, s), 2.77-2.91 (1H, m), 2.16 (1H, m), 2.09 (3H, s), 2.05 (2H, m), 1.65-1.81 (1H, m), 1.27- 1.52 (4H, m), 1.17-1.27 (6H, m); LCMS: 98%, MS (ESI): m/z 603.3 [M + H]+
136		Yellow powder; 1H NMR (400 MHz, CD3OD) δ ppm 8.66 (1H, d, J = 1.60 Hz), 8.43 (1H, d, J = 6.40 Hz), 8.18-8.32 (1H, m), 7.80-7.87 (3H, m) 7.65-7.75 (1H, m), 7.53-7.63 (3H, m), 6.95-7.09 (1H, m), 6.72 (1H, d, J = 15.20 Hz), 4.92-5.01 (1H, m), 4.76-4.82 (1H, m), 4.07 (2H, d, J = 7.20 Hz), 3.36 (3H, s), 3.22-3.26 (1H, m), 3.11-3.20 (2H, m), 3.01-3.09 (2H, m), 2.96 (6H, s), 2.78-2.88 (1H, m), 1.96-2.16 (3H, m), 1.70-1.85 (2H, m), 1.32-1.51 (2H, m), 1.18 (6H, t, J = 6.40 Hz), 1.00-1.12 (2H, m); HPLC: 96.4% MS (ESI): m/z 662.4 [M + H]+
137		White powder; 1H NMR (CDCl3, 400 MHz): δ 8.56 (1H, m), 8.40 (2H, m), 7.41-7.88 (9H, m), 5.81-6.01 (1H, m), 5.33 (1H, dd, J = 15.2, 3.6 Hz), 4.74-5.21 (2H, m), 4.19 (1H, m), 2.84-3.36 (5H, m), 1.91 (4H, m), 1.26 (6H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 581.3 [M + H]+
138		Yellow solid; 1H NMR (400 MHz, CD3OD) δ =8.74 (d, J = 7.2 Hz, 1H), 8.25 (d, J = 8.4 Hz, 1H), 7.71-7.64 (m, 2H), 7.64-7.58 (m, 2H), 7.49-7.41 (m, 2H), 7.31 (d, J = 6.8 Hz, 1H), 6.94-6.84 (m, 1H), 6.78-6.71 (m, 1H), 4.91 (s, 1H), 4.83 (br s, 1H), 4.02 (d, J = 7.0 Hz, 2H), 3.37 (m, 2H), 3.11 (br d, J = 5.8 Hz, 2H), 2.97-2.84 (m, 9H), 2.62 (s, 3H), 1.84 (br d, J = 13.8 Hz, 2H), 1.48-1.37 (m, 2H), 1.26 (d, J = 7.2 Hz, 6H); LCMS: 100%, MS (ESI): m/z 647.4 [M + H]+
139		White solid; 1H NMR (400 MHz, CD3OD) δ = 7.83 (s, 1H), 7.43 (m, 1H), 7.42-7.38 (m, 2H), 7.37-7.31 (m, 2H), 7.04 (t, J = 7.8 Hz, 1H), 6.94-6.82 (m, 1H), 6.80-6.73 (m, 1H), 6.43 (s, 1H), 5.03 (s, 2H), 4.04 (d, J = 7.0 Hz, 2H), 3.39- 3.34 (m, 2H), 3.24 (br d, J = 12.5 Hz, 2H), 3.00 (br d, J = 6.8 Hz, 1H), 2.96 (s, 6H), 2.73 (m, 2H), 2.57 (s, 3H), 1.82 (m, 3H), 1.38 (m, 2H), 1.31 (d, J = 7.0 Hz, 6H); LCMS: 100%, MS (ESI): m/z 635.4 [M + H]+
140		White powder; 1H NMR (400 MHz, CD3OD) δ = 7.96 (d, J = 1.6 Hz, 1H), 7.76 (s, 1H), 7.54-7.51 (m, 1H), 7.48-7.45 (m, 1H), 7.25-7.17 (m, 2H), 6.95 (m, 1H), 6.88-6.83 (m, 1H), 6.77 (d, J = 8.4 Hz, 1H), 6.62 (m, 1H), 6.50 (d, J = 3.2 Hz, 1H), 4.84-4.79 (m, 1H), 4.66 (m, 1H), 4.08-3.97 (m, 3H), 3.38 (s, 3H), 3.22 (br s, 1H), 2.97 (s, 6H), 2.90-2.84 (m, 1H), 2.67-2.61 (m, 3H), 2.18-2.06 (m, 2H), 1.99 (m, 2H), 1.31-1.22 (m, 10H); LCMS: 100%, MS (ESI): m/z 650.4 [M + H]+
141		Gray solid; 1H NMR (400 MHz, CD3OD) δ = 7.85 (s, 1H), 7.47-7.35 (m, 4H), 7.19 (d, J = 7.9 Hz, 1H), 7.11-7.02 (m, 1H), 6.49 (br s, 1H), 5.57-5.39 (m, 1H), 5.24 (dd, J = 3.4, 15.0 Hz, 1H), 4.95 (m, 2H), 4.12-4.00 (m, 1H), 3.86 m, 1H), 3.75 (m, 1H), 3.54-3.41 (m, 2H), 3.21 (m, 2H), 3.04 (m, 2H), 2.83 (s, 1H), 2.54 (s, 3H), 1.31 (d, J = 6.9 Hz, 6H); LCMS: 100%, MS (ESI): m/z 598.3 [M + H]+
142		Yellow powder; 1H NMR (400 MHz, CD3OD) δ ppm 8.68 (1H, s), 8.41 (1 H, d, J = 6.40 Hz), 8.25 (1H, d, J = 6.40 Hz), 7.78-7.90 (3H, m), 7.68 (1 H, t, J = 6.40 Hz), 7.51- 7.61 (3H, m), 6.95-7.11 (1H, m), 6.72 (1H, d, J = 15.20 Hz), 4.95-5.02 (1 H, m) 4.73-4.83 (1H, m), 4.07 (2 H, d, J = 7.20 Hz), 3.43-3.54 (1H, m), 3.37 (3H, s) 3.25-3.31 (2H, m), 2.96 (6H, s), 2.77-2.87 (1H, m) 1.55 -2.11 (5H, m), 1.2-1.44 (H, m), 1.06-1.22 (8H, m); HPLC: 98.5% MS (ESI): m/z 662.4 [M + H]+
143		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.62 (1H, s) 8.45 (1H, d, J = 6.40 Hz), 8.28 (1H, d, J = 6.80 Hz), 7.84-7.93 (3 H, m), 7.66-7.72 (1H, m), 7.59 (2H, d, J = 8.00 Hz), 7.52 (1H, s), 5.78-5.95 (1H, m), 5.46 (1H, dd, J = 14.80, 3.60 Hz), 4.95-5.02 (1H, m), 4.71-4.82 (1H, m), 3.50-3.59 (1H,m), 3.06 (2H, d, J = 6.40 Hz), 2.78- 2.87 (1H, m), 2.74 (3H, s), 1.68-1.78 (1H, m), 1.25-1.53 (4H, m), 1.12-1.23 (6H, m), 1.87-2.18 (4H, m); HPLC: 98.6% MS (ESI): m/z 686.3 [M + H]+
144		White solid; 1H NMR (CDCl3, 400 MHz,) δ 9.43 (1 H, s) 8.53 (1 H, d, J = 5.2 Hz) 8.47 (1 H, d, J = 9.2 Hz) 8.30 (1 H, d, J = 2.8 Hz) 7.60 (1 H, dd, J = 9.2, 2.8 Hz) 7.56 (1 H, s) 7.46 (1 H, s) 6.47 (1 H, d, J = 5.2 Hz) 4.07 (6 H, s) 3.10-3.13 (1 H, m) 3.08 (1 H, d, J = 3.2 Hz) 3.05 (2 H, d, J = 8.8 Hz) 2.62-2.75 (2 H, m) 1.73-1.80 (2 H, m) 1.02 (3 H, t, J = 7.6 Hz); LCMS: 98.0%, MS (ESI): m/z 531.3 [M + H]+
145		Yellow solid; 1H NMR (400 MHz, CD3OD) δ = 8.70 (s, 1H), 8.45 (d, J = 6.5 Hz, 1H), 8.26 (d, J = 6.8 Hz, 1H), 7.91 (br s, 2H), 7.81 (dd, J = 2.0, 9.0 Hz, 1H), 7.74- 7.68 (m, 1H), 7.64-7.58 (m, 2H), 7.56 (s, 1H), 7.04 (td, J = 7.2, 15.0 Hz, 1H), 6.73 (d, J = 15.3 Hz, 1H), 5.08 (m, 1H), 4.85-4.78 (m, 1H), 4.09 (d, J = 7.3 Hz, 2H), 3.69 (m, 1H), 3.17-3.06 (m, 1H), 2.98 (s, 6H), 2.91-2.81 (m, 1H), 2.78 (s, 3H), 2.28 m, 1H), 2.19 (m, 2H), 1.85 (m, 1H), 1.77-1.66 (m, 1H), 1.58 (m, 2H), 1.52-1.38 (m, 1H), 1.23-1.16 (m, 6H); LCMS: 100%, MS (ESI): m/z 647.4 [M + H]+
146		Yellow powder; 1H NMR (400 MHz, CD3OD) δ 8.59 (1H, s), 8.45 (1H, d, J = 6.00 Hz), 8.20 (1H, d, J = 5.20 Hz), 7.77-7.96 (3H, m), 7.64-7.71 (1H, m), 7.48-7.61 (3H, m), 5.73-5.94 (1H, m), 5.45 (1H, dd, J = 14.80, 3.60 Hz), 5.05-5.15 (1H, d, J = 15.56 Hz), 4.70-4.78 (1H, m), 3.60- 3.75 (1H, m), 3.04-3.16 (1H, m), 2.82-2.88 (1H, m), 2.76 (3H, s), 2.07-2.35 (3H, m), 1.37-1.92 (5H, m), 1.18 (6H, d, J = 6.80 Hz); HPLC: 100% MS (ESI): m/z 608.3 [M + H]+
147		Light yellow solid; 1H NMR (400 MHz, CD3OD) δ = 8.67 (d, J = 2.0 Hz, 1H), 8.42 (d, J = 6.8 Hz, 1H), 8.24 (br d, J = 6.6 Hz, 1H), 7.90-7.78 (m, 3H), 7.69 (t, J = 7.4 Hz, 1H), 7.64-7.55 (m, 3H), 7.07-6.98 (m, 1H), 6.71 (d, J = 15.4 Hz, 1H), 5.06-4.95 (m, 1H), 4.79 (br s, 1H), 4.07 (d, J = 7.3 Hz, 2H), 2.96 (s, 6H), 2.84 (br d, J = 6.3 Hz, 1H), 2.18-1.90 (m, 5H), 1.82-1.55 (m, 3H), 1.22-1.15 (m, 6H); LCMS: 94.6%, MS (ESI): 654.6 m/z [M + H]+
148		R form; white powder; 1H-NMR (CD3OD, 400 MHz): δ 8.62-8.65 (1H, m), 8.44-8.49 (1H, m), 8.20-8.24 (1H, m), 7.79-7.90 (3H, m), 7.65-7.71 (2H, m), 7.54-7.61 (2H, m), 5.85 (1H, dd, J = 46.4, 3.6 Hz), 5.44 (1H, dd, J = 14.8, 3.6 Hz), 5.03-5.13 (1H, m), 4.65-4.76 (1H, m), 3.81-4.12 (3H, m), 3.32-3.61 (3H, m), 2.78-3.21 (4H, m), 1.16-1.21 (6H, m); HPLC: 97.5%, MS (ESI): 596.5 m/z [M + H]+
149		S form; white powder; 1H-NMR (CD3OD, 400 MHz): δ 8.62-8.65 (1H, m), 8.44-8.49 (1H, m), 8.20-8.24 (1H, m), 7.79-7.90 (3H, m), 7.65-7.71 (2H, m), 7.54-7.61 (2H, m), 5.85 (1H, dd, J = 46.4. 3.6 Hz), 5.44 (1H, dd, J = 14.8, 3.6 Hz), 5.03-5.13 (1H, m), 4.65-4.76 (1H, m), 3.81-4.12 (3H, m), 3.32-3.61 (3H, m), 2.78-3.21 (4H, m), 1.16-1.21 (6H, m); HPLC: 95.4%, MS (ESI): 596.5 m/z [M + H]+
150		White solid; 1H NMR (400 MHz, CD3OD) δ ppm 1.19- 1.28 (m, 6 H) 1.69-2.05 (m, 2 H) 2.07-2.32 (m, 2 H) 2.84- 2.94 (m, 1 H) 2.98 (s, 6 H) 3.04-3.12 (m, 1 H) 3.36-3.60 (m, 2 H) 4.09 (d, J = 7.03 Hz, 2 H) 4.32 (br s, 1 H) 4.70 (br d, J = 16.06 Hz, 0.5 H) 4.94-5.10 (m, 2 H) 5.35 (br d, J = 14.81 Hz, 0.5 H) 6.68-6.77 (m, 1 H) 7.00-7.10 (m, 1 H) 7.58-7.67 (m, 2 H) 7.67-7.77 (m, 2 H) 7.79-7.97 (m, 3 H) 8.20-8.33 (m, 1 H) 8.47 (dd, J = 16.31, 6.78 Hz, 1 H) 8.71 (s, 1 H); LCMS: 100.0%. MS (ESI): m/z 619.3 [M + H]+
151		White powder; 1H NMR (400 MHz, CD3OD) δ 8.67 (s, 1H), 8.40-8.50 (m, 1H), 8.13-8.29 (m, 1H) 7.82-7.88 (m, 2H), 7.70-7.76 (m, 1H), 7.60-7.67 (m, 1H), 7.51- 7.58 (m, 1H), 7.41-7.48 (m,1 H), 7.30-7.39 (m, 1H), 6.95-7.11 (m, 1H), 6.64-6.80 (m, 1H), 5.30-5.42 (m, 1H), 4.99-5.09 (m, 1H), 4.96-5.09 (m, 1H), 4.20-4.42 (m, 1H), 4.07 (d, J = 7.20 Hz, 2H), 2.80-3.05 (m, 9H), 2.15-2.25 (m, 1H), 1.99-2.08 (m, 1H), 1.41-1.47 (m, 3H), 1.31-1.36 (m, 2H), 1.21-1.26 (m, 6 H); HPLC: 97.5% MS (ESI): m/z 633.4 [M + H]+
152		Yellow powder; 1H NMR (CD3OD, 400 MHz): δ 8.61 (1H, dd, J = 14.8, 2 Hz), 8.39 (1H, m), 8.16 (1H, t, J = 6.4 Hz), 7.77-7.85 (2H, m), 7.62-7.77 (3H, m), 7.50-7.61 (2H, m), 6.97-7.08 (1H, m), 6.72 (1H, d, J = 15.6 Hz), 5.23 (1H, m), 5.00 (1H, t, J = 15.6 Hz), 4.62 (1H, dd, J = 15.6, 2.8 Hz), 4.07 (2H, d, J = 7.2 Hz), 3.37-3.56 (2H, m), 3.11-3.28 (2H, m), 2.96 (6H, s), 2.82-2.91 (1H, m), 1.78-2.21 (4H, m), 1.12-1.27 (6H, m); LCMS: 99%, MS (ESI): m/z 620.3 [M + H]+
153		Brown powder; 1H NMR (400 MHz, CD3OD) δ 8.40-8.49 (m, 2H), 7.86 (s, 1H), 7.80 (d, J = 6.00 Hz, 1H), 7.71-7.76 (m, 1H), 7.67 (t, J = 7.60 Hz, 1H), 7.60 (t, J = 7.20 Hz, 1H), 7.50 (s, 2H), 7.43 (d, J = 6.80 Hz, 1H), 6.90-7.05 (m, 1H), 6.66 (d, J = 15.20 Hz, 1H), 5.80 (s, 1H), 4.90- 5.05 (m, 1 H) 4.55-4.65 (m, 1H), 4.05 (d, J = 7.20 Hz, 2H), 3.03-3.14 (m, 1H), 2.96 (s, 6H), 2.46 (s, 3H), 1.26 (d, J = 6.80 Hz, 6H); HPLC: 100% MS (ESI): m/z 534.3 [M + H]+
154		Yellow solid; 1H NMR (400 MHz, CD3OD) δ ppm 1.20- 1.25 (m, 6 H) 1.43 (br s, 3 H) 1.63-1.90 (m, 2 H) 2.06 (s, 3 H) 2.11-2.26 (m, 1 H) 2.79-2.93 (m, 2 H) 2.98 (s, 6 H) 3.20-3.28 (m, 1 H) 4.09 (d, J = 7.28 Hz, 2 H) 4.93-5.39 (m, 2 H) 6.71 (dd, J = 15.31, 6.53 Hz, 1 H) 6.94-7.12 (m, 1 H) 7.57 (br s, 1 H) 7.68 (br s, 3 H) 7.82 (br s, 2 H) 8.12 (br s, 1 H) 8.38 (br s, 1 H) 8.64 (s, 1 H); LCMS: 100.0%, MS (ESI): m/z 633.4 [M + H]+
155		Yellow powder; 1H NMR (400 MHz, CD3OD) δ = 8.49 (s, 1H), 8.32 (br d, J = 6.3 Hz, 1H), 7.86 (br d, J = 6.0 Hz, 1H), 7.76-7.68 (m, 2H), 7.62-7.54 (m, 2H), 7.51 (br s, 2H), 7.44 (br d, J = 7.8 Hz, 1H), 7.05-6.94 (m, 1H), 6.64 (d, J = 15.1 Hz, 1H), 5.00 (br d, J = 15.1 Hz, 1H), 4.57 (br s. 1H), 4.02 (d, J = 7.3 Hz, 2H), 3.55 (br s, 3H), 3.38 (s, 3H), 3.28-3.21 (m, 1H), 3.23 (br s, 1H), 3.12-2.96 (m, 1H), 3.03 (br s, 1H), 2.84 (br s, 1H), 2.20-1.93 (m, 5H), 1.85 (br s, 3H), 1.56 (br s, 1H), 1.45-1.25 (m, 5H), 1.19 (d, J = 7.0 Hz, 6H); LCMS: 100%, MS (ESI): 688.4 m/z [M + H]+
156		White solid; 1H NMR (400 MHz, CD3OD) δ = 8.57 (s, 1H), 8.47 (d, J = 6.5 Hz, 1H), 8.23 (br s, 1H), 7.93-7.79 (m, 3H), 7.78-7.65 (m, 2H), 7.59 (br d, J = 9.0 Hz, 2H), 5.95-5.86 (m, 2H), 5.81 (d, J = 3.6 Hz, 1H), 5.46 (dd, J = 3.6, 14.9 Hz, 1H), 4.95-4.94 (m, 1H), 4.96-4.93 (m, 1H), 4.97-4.93 (m, 1H), 4.93 (br s, 1H), 4.95-4.92 (m, 1H), 4.95-4.91 (m, 1H), 4.87-4.86 (m, 1H), 4.86-4.86 (m, 1H), 4.83 (br s, 1H), 4.84-4.82 (m, 1H), 4.85-4.81 (m, 1H), 4.84-4.81 (m, 1H), 3.04 (td, J = 7.0, 13.7 Hz, 1H), 2.49 (s, 3H), 1.25 (dd, J = 4.3, 6.8 Hz, 6H); LCMS: 100%, MS (ESI): 495.1 m/z [M + H]+
157		3S, 4S form, white solid; 1H NMR (400 MHz, CD3OD) δ ppm 1.11-1.25 (m, 6 H) 1.28-1.64 (m, 1 H) 1.53 (br s, 1 H) 1.87 (br d, J = 11.04 Hz, 1 H) 1.96-2.14 (m, 1 H) 2.88 (br d, J = 6.02 Hz, 3 H) 3.35-3.78 (m, 5 H) 4.57-4.91 (m, 2 H) 5.11 (br t, J = 15.56 Hz, 2 H) 5.46 (dd, J = 14.93, 3.39 Hz, 1 H) 5.81 (br s, 1 H) 5.92 (br s, 1 H) 7.52-7.93 (m, 7 H) 8.19 (br s, 1 H) 8.47 (br s, 1 H) 8.62 (br s, 1 H); LCMS: 100%, MS (ESI): 610.1 m/z [M + H]+
158		3S, 4R form, yellow powder; 1H NMR (400 MHz, CD3OD) δ ppm 8.57 (s, 1H), 8.44 (s, 1H), 8.11 ( d, J = 6.40 Hz, 1H), 7.74-7.88 (m, 3H), 7.58-7.70 (m, 2H), 7.51-7.56 (m, 2H), 5.75-5.95 (m, 1H), 5.44 (dd, J = 14.80, 3.60 Hz, 1H), 4.99-5.17 (m, 1H), 4.65 (d, J = 14.40 Hz, 1H), 4.05 (d, J = 12.80 Hz, 1 H), 3.34-3.48 (m, 2H), 3.20-3.30 (m, 2H), 2.82-3.15 (m, 3H), 1.78-2.01 (m, 2H), 1.63-1.73 (m, 1H), 1.16-1.22 (m, 6H); HPLC: 96.2% MS (ESI): m/z 610.3 [M + H]+
159		Yellow powder; 1H NMR (400 MHz, CD3OD) δ ppm 8.58 (dd, J = 19.60, 2.00 Hz, 1H), 8.36-8.43 (m, 1H), 8.13 (d, J = 6.40 Hz, 1H), 7.72-7.82 (m, 3H), 7.59-7.69 (m, 2H), 7.51-7.57 (m, 2H), 5.74-5.95 (m, 1H), 5.44 (dd, J = 14.80, 3.60 Hz, 1H), 5.20 (s, 1H), 5.03 (d, J = 15.20 Hz, 1H), 4.56 (t, J = 16.00 Hz, 1H), 3.37-3.54 (m, 2H), 3.10-3.27 (m, 2H), 2.80-2.92 (m, 1H), 1.84-2.15 (m, 4H) 1.16-1.26 (m, 6H); HPLC: 99.3% MS (ESI): m/z 581.1 [M + H]+
160		3R,4R and 3S, 4S form mixture; yellow solid; 1H NMR (400 MHz, CD3OD) δ ppm 8.59 (s, 1H), 8.46 ( s, 1H), 8.05-8.25 (m, 1H), 7.75-7.87 (m, 3H), 7.62-7.70 (m, 2H), 7.49-7.58 (m, 2H), 5.71-5.98 (m, 1H), 5.44 (dd, J = 14.80, 3.60 Hz, 1H), 5.12 (d, J = 14.80 Hz, 1H), 4.50-4.65 (m, 1H), 3.51-3.79 (m, 2H), 3.35-3.46 (m, 3H), 2.95-3.05 (m, 1H), 2.75-2.84 (m, 2H), 2.02 (d, J = 11.20 Hz, 1H), 1.75-1.84 (m, 1H), 1.50-1.62 (m, 1H), 1.15-1.30 (m, 6H); HPLC: 99.2% MS (ESI): m/z 610.3 [M + H]+
161		Yellow solid; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.54 (s, 1 H) 8.85 (br s, 2 H) 8.52 (d, J = 5.77 Hz, 1 H) 8.44- 8.49 1 H) 8.47 (d, J = 1.76 Hz, 1 H) 8.13 (br s, 1 H) 7.86 (dd, J = 9.03, 2.01 Hz, 1 H) 7.81 (d, J = 6.02 Hz, 1 H) 7.58-7.64 (m, 3 H) 7.51-7.57 (m, 1 H) 7.45-7.51 (m, 1 H) 7.39 (d, J = 7.53 Hz, 1 H) 6.58 (br s, 1 H) 5.73-5.91 (m, 1 H) 5.47 (dd, J = 15.69, 3.89 Hz, 1 H) 4.49 (br s, 2 H) 4.04 (br s, 1 H) 3.22-3.28 (m, 2 H) 2.75-2.99 (m, 4 H) 1.93 (m, 2 H) 1.76 (m, 1 H) 1.60 (m, 1 H) 1.24 (d, J = 7.03 Hz, 6 H); HPLC: 95.8%, MS (ESI): 580.1 m/z [M + H]+
162		3R, 4S form white solid; 1H NMR (400 MHz, CD3OD) δ ppm 8.67 (s, 1 H) 8.52 (d, J = 6.78 Hz, 1 H) 8.31 (d, J = 6.53 Hz, 1 H) 7.80-8.00 (m, 3 H) 7.54-7.76 (m, 4 H) 5.80- 5.98 (m, 1 H) 5.48 (dd, J = 14.81, 3.76 Hz, 1 H) 5.12 (br dd, J = 15.56, 7.28 Hz, 1 H) 4.74 (br dd, J = 15.69, 2.89 Hz, 1 H) 4.13 (br s, 1 H) 3.35-3.54 (m, 3 H) 2.96-3.23 (m, 2 H) 2.87 (dt, J = 13.61, 6.87 Hz, 1 H) 1.59-2.12 (m, 3 H) 1.14-1.28 (m, 6 H) 1.14-1.28 (m, 1 H); HPLC: 97.8% (254 nm), MS (ESI): m/z 610.2 [M + H]+
163		Yellow solid; 1H NMR (400 MHz, CD3OD) δ = 8.67 (br s, 1H), 8.52-8.45 (m, 1H), 8.33-8.20 (m, 1H), 7.95 (br s, 1H), 7.90-7.66 (m, 4H), 7.65-7.57 (m, 2H), 5.96-5.79 (m, 1H), 5.46 (dd, J = 4.0, 13.6 Hz, 1H), 5.02 (br s, 1H), 5.15- 4.93 (m, 1H), 4.62 (br d, J = 15.3 Hz, 1H), 4.34 (br s, 1H), 3.62-3.35 (m, 1H), 3.29-3.21 (m, 1H), 3.09-2.79 (m, 2H), 2.35-2.10 (m, 1H), 2.08-1.65 (m, 3H), 1.44 (br d, J = 6. Hz, 3H), 1.25-1.17 (m, 6H); LCMS: 100%, MS (ESI): m/z 594.3 [M + H]+
164		White powder; 1H NMR (DMSO-d6, 400 MHz) δ 10.43 (1 H, s) 8.51 (1 H, d, J = 6.0) 8.41 (1 H, d, J = 2.0 Hz) 7.91 (1 H, s) 7.73-7.81 (2 H, m) 7.56-7.62 (3 H, m) 7.4 -7.52 (2 H, m) 7.31-7.37 (1 H, m) 6.22 (1 H, s) 5.68-5.86 (1 H, m) 5.44 (1 H, dd, J = 15.6, 3.6 Hz) 4.89 (1 H, s) 4.45 (2 H, s) 3.31-3.35 (2 H, m) 2.88 (2 H, dq, J = 14.0, 7.2 Hz) 2.70- 2.80 (1 H, m) 2.26 (3 H, s) 1.80-2.05 (2 H, m) 1.62 (1 H, d, J = 13.2 Hz) 1.23-1.43 (2 H, m) 1.21 (6 H, d, J = 6.8 Hz); LCMS: 100%, MS (ESI): m/z 624.3 [M + H]+
165		White powder; 1H NMR (DMSO-d6, 400 MHz) δ 10.72 (1 H, s) 8.79 (1 H, d, J = 6.0 Hz) 8.71 (1 H, d, J = 2.4 Hz) 8.40 (1 H, s) 8.06 (1 H, dd, J = 9.2, 2.0 Hz) 8.01 (1 H, d, J = 6.0 Hz) 7.93 (1 H, s) 7.82-7.90 (2 H, m) 7.70-7.82 (2 H, m) 7.64 (1 H, dd, J = 7.2, 1.6 Hz) 6.18 (1 H, d, J = 9.6 Hz) 5.99-6.15 (1 H, m) 5.76 (1 H,, J = 15.6, 3.6 Hz) 4.69- 4.84 (3 H, m) 4.58-4.66 (1 H, m) 3.54-3.68 (2 H, m) 3.12- 3.26 (2 H, m) 3.04 (1 H, d, J = 11.2 Hz) 2.91-2.99 (1 H, m) 2.50 (3 H, s) 2.13-2.24 (1 H, m) 2.05 (1 H, t, J = 10.0 Hz) 1.70 (1 H, d, J = 10.4 Hz) 1.56 (1 H, s) 1.54-1.59 (1 H, m) 1.53 (6 H, d, J = 7.2 Hz); LCMS: 100%, MS (ESI): m/z 636.3 [M + H]+
166		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.18 (6 H, d, J = 6.78 Hz) 1.61 (1 H, br d, J = 9.03 Hz) 1.81- 1.99 (3 H, m) 2.86 (4 H, dt, J = 13.68, 6.96 Hz) 4.10 (1 H, br s) 4.67 (2 H, br s) 5.51 (1 H, dd, J = 15.56, 3.76 Hz) 5.79-5.98 (1 H, m) 7.47 (1 H, d, J = 7.53 Hz) 7.53-7.59 (3 H, m) 7.68 (1 H, t, J = 7.40 Hz) 7.73-7.79 (1 H, m) 7.93 (1 H, dd, J = 9.29, 2.01 Hz) 8.12 (1 H, d, J = 6.27 Hz) 8.47 (1 H, d, J = 6.27 Hz) 8.56 (1 H, d, J = 1.76 Hz) 9.11 (2 H, br s) 10.80 (1 H, br s); LCMS : 99.72%, MS (ESI): m/z 580.3 [M + H]+
167		White solid; 1H NMR (400 MHz, CD3OD) δ ppm 8.27 (d, J = 6.02 Hz, 1 H) 8.24 (d, J = 1.76 Hz, 1 H) 7.59-7.64 (m, 1 H) 7.57 (t, J = 2.89 Hz, 2 H) 7.54 (td, J = 7.59, 1.38 Hz, 1 H) 7.46 (td, J = 7.53, 1.25 Hz, 1 H) 7.40-7.44 (m, 1 H) 7.34-7.39 (m, 1 H) 7.29 (dd, J = 7.53, 1.00 Hz, 1 H) 6.81- 6.93 (m, 1 H) 6.53 (d, J = 15.06 Hz, 1 H) 5.03 (br d, J = 14.81 Hz, 1 H) 4.32 (d, J = 14.81 Hz, 1 H) 3.96 (dd, J = 7.28, 1.00 Hz, 2 H) 2.96 (quin, J = 6.90 Hz, 1 H) 2.88 (s, 6 H) 2.12 (s, 3 H) 1.15 (t, J = 7.03 Hz, 6 H); HPLC: 98.1%, MS (ESI): 535.1 m/z [M + H]+
168		White powder; 1H NMR (400 MHz, DMSO-d6) δ 11.11 (1 H, s), 10.67-11.00 (1 H, d, J = 44.0 Hz), 9.63 (1 H, s), 8.32- 8.78 (3 H, m), 7.32-8.00 (7 H, m), 5.95 (1 H, dd, J = 15.60, 4.00 Hz), 5.60 (1 H, dd, J = 15.60, 4.00 Hz), 4.79-5.01 (1 H, m), 4.44-4.65 (1 H, m), 3.80-3.95 (1 H, m), 3.04-3.41 (5 H, m), 2.75-2.90 (2 H, m), 2.60-2.70 (1 H, m), 1.57- 1.93 (3 H, m), 1.28 (6 H, br d, J = 6.40 Hz) 1.13 (6 H, t, J = 6.40 Hz); HPLC: 97.9%, MS (ESI): m/z 652.4 [M + H]+
169		White powder; 1H NMR (400 MHz, DMSO-d6) δ 10.90- 11.31 (2 H, m), 10.11 (1 H, br s), 9.40 (1 H, br s), 8.59- 8.69 (1 H, m), 8.44-8.55 (1 H, m), 8.17-8.29 (1 H, m), 7.95-8.09 (1 H, m), 7.83 (1 H, d, J = 7.6 Hz), 7.73 (1 H, t, J = 7.6 Hz), 7.46-7.66 (4 H, m), 5.83-6.12 (1 H, m), 5.53 (1 H, dd, J = 15.6, 4.0 Hz), 3.75-3.94 (1 H, m), 3.64 (1 H, d, J = 12.0 Hz), 3.32-3.45 (2 H, m), 3.02-3.24 (3 H, m), 2.88-2.96 (1 H, m), 2.58-2.84 (2 H, m), 1.92 (1 H, d, J = 10.0 Hz), 1.60-1.75 (2 H, m), 1.33 (3 H, t, J = 4.0 Hz), 1.19 (6 H, d, J = 7.2 Hz); HPLC: 100%, MS (ESI): m/z 638.4 [M + H]+
170		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (6 H, d, J = 6.78 Hz) 2.86 (2 H, t, J = 6.02 Hz) 2.93 (1 H, dt, J = 13.80, 6.90 Hz) 3.89 (2 H, t, J = 6.02 Hz) 4.52 (2 H, br s) 4.70 (2 H, s) 5.44 (1 H, dd, J = 15.56, 3.76 Hz) 5.68- 5.88 (1 H, m) 7.18 (1 H, dd, J = 7.78, 4.77 Hz) 7.35 (1 H, dd, J = 7.40, 1.38 Hz) 7.41-7.53 (3 H, m) 7.56 (1 H, d, J = 9.29 Hz) 7.59-7.63 (2 H, m) 7.68 (1 H, d, J = 5.77 Hz) 7.77 (1 H, dd, J = 9.16, 2.13 Hz) 8.08 (1 H, br s) 8.33-8.37 (1 H, m) 8.42 (1 H, d, J = 2.01 Hz) 8.47 (1 H, d, J = 5.77 Hz) 10.41 (1 H, br s); LCMS: 100% MS (ESI): m/z 614.3 [M + H]+
171		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ 10.75 (1 H, s), 9.05-9.30 (2 H, m), 8.56 (1 H, d, J = 1.6 Hz), 8.48 (1 H, d, J = 6.4 Hz), 8.07 (1 H, d, J = 6.4 Hz) 7.94 (1 H, dd, J = 9.2, 2.0 Hz), 7.73 (1 H, d, J = 7.6 Hz), 7.51-7.68 (4 H, m), 7.50-7.51 (1 H, m), 7.44-7.47 (1 H, m), 5.85 (1 H, dd, J = 48.0, 4.0 Hz), 5.50 (1 H, dd, J = 16.0, 4.0 Hz), 4.50- 4.75 (2 H, m), 4.01-4.23 (1 H, m), 2.80-3.00 (3 H, m), 1.71-1.89 (4 H, m), 1.38 (6 H, d, J = 16.0 Hz), 1.19 (6 H, d, J = 8.0 Hz); HPLC: 98.5%, MS (ESI): m/z 608.3 [M + H]+
172		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.71 (1 H, s) 9.04 (2 H, br s) 8.55 (1 H, d, J = 1.76 Hz) 8.49 (1 H, d, J = 6.27 Hz) 8.02 (1 H, d, J = 6.27 Hz) 7.92 (1 H, dd, J = 9.16, 1.88 Hz) 7.68-7.74 (1 H, m) 7.50-7.67 (4 H, m) 7.42-7.47 (1 H, m) 5.75-5.95 (1 H, m) 5.50 (1 H, dd, J = 15.56, 4.02 Hz) 4.60 (2 H, br s) 4.07 (1 H, br s) 2.88 (4 H, dt, J = 13.80, 6.90 Hz) 1.93 (2 H, br d, J = 10.29 Hz) 1.80 (1 H, br d, J = 13.30 Hz) 1.61 (1 H, br d, J = 9.54 Hz) 1.21 (7 H, d, J = 7.03 Hz); LCMS: 100%, MS (ESI): m/z 580.1 [M + H]+
173		Pink powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.20 (6 H, br d, J = 6.78 Hz) 1.38-1.82 (4 H, m) 1.83-2.44 (6 H, m) 2.76-3.00 (2 H, m) 3.49-3.93 (1 H, m) 4.42 (2 H, br s) 5.52 (1 H, dd, J = 15.81, 3.76 Hz) 5.73-5.89 (1 H, m) 5.94- 6.77 (1 H, m) 7.34 (1 H, br d, J = 7.28 Hz) 7.41-7.55 (3 H, m) 7.63 (2 H, s) 7.76-7.86 (2 H, m) 8.26-8.61 (3 H, m) 10.70 (1 H, br s); LCMS: 100%, MS (ESI): m/z 594.3 [M + H]+
174		Yellow solid; 1H NMR (DMSO-d6, 400 MH) δ 8.52 (1 H, d, J = 5.6 Hz) 8.44 (1 H, d, J = 2.0 Hz) 7.92 (1 H, s) 7.83 (1 H, dd, J = 9.2, 2.4 Hz) 7.74 (1 H, d, J = 5.6 Hz) 7.55- 7.66 (3 H, m) 7.40-7.53 (2 H, m) 7.35 (1 H, dd, J = 7.6, 1.2 Hz) 6.04 (1 H, s) 5.68-5.87 (1 H, m) 5.45 (1 H, dd, J = 15.6, 3.6 Hz) 4.46 (2 H, s) 3.59 (1 H, s) 2.89 (2 H, dt, J = 14.0, 6.8 Hz) 2.55-2.61 (1 H, m) 1.69 (1 H, s) 1.57 (1 H, q, J = 9.2 Hz) 1.42-1.51 (1 H, m) 1.25-1.36 (1 H, m) 1.22 (6 H, d, J = 6.8 Hz) 1.06 (6 H, d, J = 4.8 Hz); LCMS: 100%, MS (ESI): m/z 608.3 [M + H]+
175		White powder; 1H NMR (DMSO-d6, 400 MHz) δ 8.52 (1 H, d, J = 6.0 Hz) 8.44 (1 H, d, J = 1.2 Hz) 7.93 (1 H, s) 7.83 (1 H, dd, J = 8.8, 2.0 Hz) 7.74 (1 H, d, J = 5.6 Hz) 7.56-7.65 (3 H, m) 7.41-7.52 (2 H, m) 7.35 (1 H, d, J = 6.4 Hz) 6.05 (1 H, s) 5.69-5.87 (1 H, m) 5.45 (1 H, dd, J = 15.6, 3.6 Hz) 4.46 (2 H, s) 3.59 (1 H, s) 2.86-2.93 (2 H, m) 2.57 (1 H, dd, J = 12.4, 7.2 Hz) 1.69 (1 H, s) 1.51- 1.63 (1 H, m) 1.43-1.51 (1 H, m) 1.25-1.33 (1 H, m) 1.22 (6 H, d, J = 7.2 Hz) 1.06 (6 H, d, J = 4.0 Hz); LCMS: 98.4%, MS (ESI): m/z 608.3 [M + H]+
176		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.19-1.28 (8 H, m) 1.73 (1 H, br s) 1.90 (2 H, br s) 1.99- 2.23 (3 H, m) 2.87 (1 H, dt, J = 14.05, 7.03 Hz) 3.11-3.14 (3 H, m) 3.54-3.69 (1 H, m) 4.11 (1 H, br s) 4.56 (2 H, br s) 5.50 (1 H, dd, J = 15.56, 4.02 Hz) 5.72-5.95 (1 H, m) 7.28-7.34 (1 H, m) 7.40-7.44 (1H, m) 7.51 (1 H, t, J = 7.28 Hz) 7.57-7.64 (4 H, m) 7.85-7.94 (2 H, m) 8.33 (1 H, s) 8.44-8.55 (2 H, m) 9.99-10.30 (1 H, m) 10.66 (1 H, br s); LCMS: 99.0%, MS (ESI): m/z 606.3 [M + H]+
177		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.22 (6 H, d, J = 6.78 Hz) 1.26 (1 H, s) 1.38-1.44 (6 H, m) 1.70-1.89 (3 H, m) 1.99-2.07 (1 H, m) 2.90 (1 H, dt, J = 13.80, 6.90 Hz) 3.14 (1 H, br s) 3.37 (1 H, br d, J = 11.54 Hz) 5.06-5.20 (1 H, m) 5.53 (1 H, dd, J = 15.69, 3.89 Hz) 5.84-5.99 (1 H, m) 7.46-7.51 (1 H, m) 7.53-7.64 (2 H, m) 7.64-7.75 (3 H, m) 7.97 (1 H, br d, J = 9.29 Hz) 8.14 (1 H, d, J = 6.53 Hz) 8.50 (1 H, d, J = 6.27 Hz) 8.60 (1 H, d, J = 2.01 Hz) 8.63 (1 H, br s) 9.04 (1 H, br s) 9.52 (1 H, br s) 10.87 (1 H, s); LCMS: 98.77%, MS (ESI): m/z 609.2 [M + H]+
178		Yellow powder; 1H NMR (DMSO-d6, 400 MHz) δ 10.39 (1 H, br s), 8.49 (1 H, d, J = 4.0 Hz), 8.45 (1 H, d, J = 4.0 Hz), 8.04 (1 H, br s), 7.73 (1 H, d, J = 4.0 Hz), 7.67-7.71 (1 H, m), 7.55-7.63 (3 H, m), 7.43-7.53 (2 H, m), 7.35 (1 H, dd, J = 8.0, 4.0 Hz), 6.47 -6.66 (1 H, m) 6.23-6.38 (2 H, m), 5.81 (1 H, dd, J = 8.0, 2.0 Hz), 4.47 (2 H, br s), 3.81 (1 H, br s), 2.78-2.90 (3 H, m), 1.63-1.79 (2 H, m), 1.43- 1.53 (2 H, m), 1.13-1.29 (12 H, m); HPLC: 97.1%, MS (ESI): m/z 590.3 [M + H]+
179		White powder; 1H NMR (DMSO-d6, 400 MHz) δ ppm 10.30 (1 H, s) 8.48 (1 H, d, J = 5.6 Hz) 8.43 (1 H, s) 8.01 (1 H, s) 7.65-7.74 (2 H, m) 7.54-7.62 (3 H, m) 7.42-7.52 (2 H, m) 7.35 (1 H, d, J = 6.8 Hz) 6.78-6.90 (1 H, m) 6.35 (1 H, d, J = 15.6 Hz) 6.18 (1 H, s) 4.46 (2 H, s) 3.69 (1 H, s) 2.85-2.95 (1 H, m) 2.67 (2 H, s) 2.50 (17 H, s) 2.22 (6 H, s) 1.90 (1 H, s) 1.71 (1 H, s) 1.49-1.66 (3 H, m) 1.40 (1 H, d, J = 9.6 Hz) 1.22 (6 H, d, J = 6.8 Hz) 1.13 (6 H, s): LCMS: 100%, MS (ESI): m/z 647.3 [M + H]+
180		White powder: 1H NMR (DMSO-d6, 400 MHz) δ ppm 10.33 (1 H, s) 8.48 (1 H, d, J = 5.6 Hz) 8.43 (1 H, d, J = 2.0 Hz) 8.06 (1 H, s) 7.66-7.74 (2 H, m) 7.54-7.62 (3 H, m) 7.42-7.52 (2 H, m) 7.35 (1 H, dd, J = 7.6, 1.2 Hz) 6.84 (1 H, dt, J = 15.6, 6.0 Hz) 6.30-6.42 (2 H, m) 4.46 (2 H, s) 3.85 (1 H, s) 3.59-3.66 (4 H, m) 2.90 (1 H, dt, J = 13.6, 6.8 Hz) 2.43-2.46 (4 H, m) 1.91 (1 H, s) 1.78 (1 H, s) 1.65 (2 H, d, J = 13.2 Hz) 1.54 (1 H, d, J = 10.4 Hz) 1.22-1.27 (12 H, m); LCMS: 100%, MS (ESI): m/z 689.4 [M + H]+
181		White powder; 1H NMR (400 MHz, DMSO-d6) δ 9.99 (1 H, s), 8.49 (1 H, d, J = 4.0 Hz), 8.43 (1 H, s), 7.99 (1 H, s), 7.80 (1 H, d, J = 8.0 Hz), 7.72 (1 H, d, J = 4.0 Hz), 7.55- 7.63 (3 H, m), 7.41-7.52 (2H, m), 7.35 (1 H, d, J = 8.0 Hz,), 6.13 (1 H, s), 5.89 (1 H, s), 5.57 (s, 1 H), 4.46 (2 H, s), 3.63 (1 H, s), 2.83-3.00 (2 H, m), 2.60-2.70 (1H, m), 2.01 (3 H, s), 1.62-1.69 (1 H, m), 1.56-1.59 (1 H, m), 1.46-1.55 (1 H, m), 1.30-1.35 (1 H, m), 1.23 (6 H, d, J = 4.0 Hz), 1.09 (6 H, s); LCMS: 100%, MS (ESI): m/z 604.3 [M + H]+
182		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.29 (s, 1 H) 8.72 (br s, 1 H) 8.28-8.52 (m, 4 H) 7.76- 7.90 (m, 1 H) 7.68 (d, J = 5.60 Hz, 1 H) 7.55-7.65 (m, 2 H) 7.49-7.53 (m, 3 H) 7.43-7.48 (m, 1 H) 7.40 (dd, J = 8.40, 4.64 Hz, 1 H) 7.33 (d, J = 6.40 Hz, 1 H) 6.40-6.59 (m, 1 H) 6.26-6.39 (m, 1 H) 5.69-5.88 (m, 1 H) 4.49 (br s, 2 H) 1.17 (d, J = 7.20 Hz, 6 H); LCMS: 100%, MS (ESI): m/z 557.5 [M + H]+
183		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.40 (br s, 1 H) 8.37-8.45 (m, 2 H) 8.19-8.26 (m, 1 H) 8.10 (d, J = 1.20 Hz, 1 H) 7.77-7.87 (m, 2 H) 7.67 (d, J = 5.60 Hz, 1 H) 7.57-7.62 (m, 1 H) 7.41-7.54 (m, 4 H) 7.37 (m, 1 H) 7.26-7.37 (m, 1 H) 7.13 (dd, J = 8.80, 3.20 Hz, 1 H) 6.42-6.60 (m, 1 H) 6.25-6.40 (m, 1 H) 5.72- 5.84 (m, 1 H) 4.47 (br s, 2 H) 2.77-2.93 (m, 1 H) 1.16 (d, J = 7.20 Hz, 6 H); LCMS: 100%, MS (ESI): m/z 1011.5 [M + H]+
184		White powder; 1H NMR (400 MHz, DMSO-d6) δ 10.39 (1 H, s), 8.53 (1 H, d, J = 4.0 Hz), 8.47 (1 H, s), 7.76 (1 H, d, J = 4.0 Hz), 7.68-7.73 (1 H, m), 7.60-7.64 (1 H, m), 7.43- 7.57 (4 H, m), 7.37 (1 H, d, J = 8.0 Hz), 7.12-7.24 (1 H, m), 6.47-6.59 (1 H, m), 6.27-6.39 (1 H, m), 6.17 (1 H, br d, J = 8.0 Hz), 5.82 (1 H, d, J = 12.0 Hz), 5.03 (1 H, s), 4.25 (2 H, br d, J = 4.0 Hz), 3.86 (1 H, br s), 2.90-2.97 (2 H, m), 2.73-2.88 (1 H, m), 1.45-1.90 (4 H, m), 1.25 (6 H, d, J = 8.0 Hz), 1.21 (6 H, s); HPLC: 98.8% (254 nm), MS (ESI): m/z 589.3 [M + H]+
185		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (6 H, d, J = 6.78 Hz) 1.52-1.64 (3 H, m) 1.92 (3 H, br s) 1.99-2.09 (3 H, m) 2.22 (5 H, s) 2.96 (1 H, dt, J = 13.55, 6.78 Hz) 3.87 (2 H, br s) 4.24 (2 H, br d, J = 6.27 Hz) 5.05 (1 H, s) 6.21 (1 H, br d, J = 6.78 Hz) 6.32-6.38 (1 H, m) 6.84 (1 H, dt, J = 15.43, 5.96 Hz) 7.11 (1 H, br s) 7.35-7.38 (1 H, m) 7.43-7.48 (1 H, m) 7.48-7.51 (1H, m) 7.52 (1 H, s) 7.53-7.57 (1 H, m) 7.58-7.61 (1 H, m) 7.65-7.69 (1 H, m) 7.74 (1 H, d, J = 5.52 Hz) 8.45 (1 H, d, J = 2.01 Hz) 8.51 (1 H, d, J = 5.77 Hz) 10.29 (1 H, s); LCMS: 97.46%, MS (ESI): m/z 653.3 [M + H]+
186		Pink powder; 1H NMR (400 MHz, DMSO-d6) δ 10.37 (1 H, s), 8.53 (1 H, d, J = 4.0 Hz), 8.47 (1 H, d, J = 2.0 Hz), 7.76 (1 H, d, J = 8.0 Hz), 7.67-7.72 (1 H, m), 7.59-7.65 (1 H, m), 7.43-7.58 (4 H, m), 7.37 (1 H, d, J = 8.0 Hz) 7.08- 7.15 (1 H, m), 6.47-6.60 (1 H, m), 6.30-6.42 (1 H, m), 6.22 (1 H, d, J = 8.0 Hz), 5.82 (1 H, dd, J = 10.00, 2.0 Hz), 5.06 (1 H, s), 4.25 (2 H, d, J = 8.0 Hz), 3.82-3.94 (1H, m), 2.91-3.00 (1 H, m), 1.85-2.10 (6 H, m), 1.51-1.65 (2 H, m), 1.26 (6 H, d, J = 4.0 Hz); HPLC: 98.0% (254 nm), MS (ESI): m/z 596.3 [M + H]+
187		White powder; 1H NMR (DMSO-d6, 400 MHz) δ 10.36 (1 H, s) 8.72 (1 H, s) 8.52 (1 H, d, J = 5.6 Hz) 8.46 (1 H, d, J = 2.0 Hz) 7.72-7.77 (2 H, m) 7.62-7.70 (3 H, m) 7.45- 7.57 (3 H, m) 7.38 (1 H, d, J = 7.2 Hz) 7.32 (1 H, s) 7.08- 7.12 (2 H, m) 6.46-6.56 (2 H, m) 6.30-6.40 (1 H, m) 5.78- 5.85 (1 H, m) 5.35 (1 H, s) 4.32 (2 H, d, J = 6.0 Hz) 4.18- 4.25 (1 H, m) 2.81 (1 H, dd, J = 13.2, 7.2 Hz) 1.90-1.96 (1 H, m) 1.67-1.79 (1 H, m) 1.56-1.65 (1 H, m) 1.35-1.42 (1 H, m) 1.32 (6 H, dd, J = 6.8, 0.8 Hz) 1.26 (1 H, d, J = 3.2 Hz) 1.11 (6 H, d, J = 12.0 Hz); LCMS: 99.6%, MS (ESI): m/z 681.4 [M + H]+
188		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.39 (s, 1 H) 9.10 (br s, 1 H) 8.99 (d, J = 2.51 Hz, 1 H) 8.54 (d, J = 5.77 Hz, 1 H) 8.48 (s, 1 H) 8.35 (br s, 1 H) 8.22-8.26 (m, 1 H) 8.20-8.22 (m, 1 H) 7.80 (s, 1 H) 7.75 (d, J = 5.77 Hz, 1 H) 7.68-7.73 (m, 2 H) 7.67 (s, 1 H) 7.59 (td, J = 7.47, 1.38 Hz, 1 H) 7.52-7.57 (m, 1 H) 7.44 (dd, J = 7.40, 1.38 Hz, 1 H) 7.30 (dd, J = 8.41, 4.64 Hz, 1 H) 6.52-6.64 (m, 1 H) 6.36-6.47 (m, 1 H) 5.85-5.93 (m, 1 H) 4.65 (br d, J = 5.02 Hz, 2 H) 3.02-3.10 (m, 1 H) 1.37 (d, J = 6.78 Hz, 6 H); HPLC: 98.7%, MS (ESI): 556.1 m/z [M + H]+
189		White powder; 1H NMR (DMSO-d6, 400 MHz) δ 8.85 (2 H, d, J = 7.6 Hz) 8.23-8.30 (2 H, m) 7.98 (1 H, s) 7.67 (1 H, d, J = 7.2 Hz) 7.39-7.56 (5 H, m) 7.32 (1 H, d, J = 7.2 Hz) 7.01 (2 H, d, J = 7.2 Hz) 6.49-6.59 (1 H, m) 6.33 (1 H, dd, J = 16.8, 2.0 Hz) 5.80 (1 H, dd, J = 10.0, 2.0 Hz) 4.71 (2 H, s) 1.31 (6 H, d, J = 6.8 Hz); LCMS: 97.2%, MS (ESI): m/z 556.3 [M + H]+
190		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.09 (6 H, d, J = 8.78 Hz) 1.25 (6 H, d, J = 7.03 Hz) 1.32-1.40 (1 H, m) 1.51-1.58 (1 H, m) 1.64-1.74 (1 H, m) 1.84-1.95 (1 H, m) 2.01 (3 H, s) 2.76 (1 H, dd, J = 12.92, 7.40 Hz) 2.94-3.00 (2 H, m) 4.51 (2 H, br s) 4.69 (1 H, tt, J = 7.78, 4.02 Hz) 5.57 (1 H, s) 5.89 (1 H, s) 7.34 (1 H, d, J = 7.03 Hz) 7.43-7.52 (2 H, m) 7.53-7.60 (2 H, m) 7.68 (1 H, d, J = 5.77 Hz) 7.73-7.79 (2 H, m) 8.40 (1 H, s) 8.45 (1 H, d, J = 5.52 Hz) 9.97 (1 H, br s); LCMS: 100%, MS (ESI): m/z 605.4 [M + H]+
191		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.65 (br s, 1 H) 7.87 (s, 1 H) 7.41-7.48 (m, 1 H) 7.31-7.41 (m, 2 H) 7.19-7.25 (m, 1 H) 7.15-7.19 (m, 1 H) 7.06-7.15 (m, 2 H) 5.13-5.32 (m, 2 H) 5.08 (br s, 1 H) 4.76 (br d, J = 17.07 Hz, 1 H) 4.53 (m 2 H) 4.32-4.45 (m, 1 H) 3.74 (m, 1 H) 3.50 (m, 1 H) 3.36 (m, 1 H) 3.15-3.18 (m, 1 H) 2.99- 3.03 (m, 1 H) 2.54 (m, 2 H) 2.04 (m, 1 H) 1.72-1.90 (m, 2 H) 1.56-1.67 (m, 1 H) 1.34 (m, 6 H) 1.29 (d, J = 7.03 Hz, 6 H); HPLC: 100%, MS (ESI): 598.4 m/z [M + H]+
192		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 9.23 (br s, 1 H) 9.09 (br s, 1 H) 8.15-8.83 (m, 1 H) 7.75 (s, 1 H) 7.47 (m, 1 H) 7.31-7.42 (m, 2 H) 7.19-7.26 (m, 1 H) 7.06- 7.19 (m, 3 H) 5.10-5.32 (m, 2 H) 4.74 (m, 1 H) 4.32- 4.70 (m, 3 H) 4.16 (br s, 1 H) 3.65-3.75 (m, 2 H) 3.34 (m, 1 H) 3.15 (m, 1 H) 2.98 (dt, J = 13.80, 6.90 Hz, 1 H) 2.87 (m, 2 H) 2.53-2.60 (m, 1 H) 2.42-2.48 (m, 1 H) 1.85-2.06 (m, 2 H) 1.71-1.85 (m, 1 H) 1.55-1.69 (m, 1 H) 1.27 (d, J = 6.78 Hz, 6 H); HPLC: 100%, MS (ESI): 569.1 m/z [M + H]+
193		White solid; 1H NMR (400 MHz, CDCl3) δ ppm 8.59 (1 H, d, J = 5.52 Hz) 8.36 (1 H, d, J = 1.76 Hz) 7.72 (1 H, s) 7.39-7.67 (7 H, m) 7.31 (1 H, dd, J = 9.03, 2.01 Hz) 7.03 (1 H, br t, J = 6.15 Hz) 6.52 (1 H, dd, J = 16.81, 1.00 Hz) 6.24-6.34 (1 H, m) 5.87 (1 H, dd, J = 10.29, 1.00 Hz) 5.61 (1 H, s) 4.28-4.59 (2 H, m) 3.13-3.23 (1 H, m) 1.28 (7 H, d, J = 6.78 Hz); LCMS: 100.0%, MS (ESI): m/z 497.2 [M + H]+
194		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.35 (br s, 1 H) 8.77 (s, 1 H) 8.48 (d, J = 5.77 Hz, 1 H) 8.42 (s, 1 H) 8.22 (br s, 1 H) 7.67-7.72 (m, 2 H) 7.59-7.66 (m, 2 H) 7.49-7.55 (m, 1 H) 7.44-7.49 (m, 1 H) 7.37 (br d, J = 7.28 Hz, 1 H) 7.23 (br d, J = 9.29 Hz, 1 H) 7.10 (t, J = 8.16 Hz, 1 H) 5.82 (br dd, J = 10.16, 1.88 Hz, 1 H) 4.57 (br s, 2 H) 4.21 (br d, J = 3.76 Hz, 1 H) 3.00-3.06 (m, 2 H) 2.79 (br dd, J = 12.80, 7.03 Hz, 1 H) 1.89-2.07 (m, 2 H) 1.67-1.77 (m, 1 H) 1.54-1.64 (m, 1 H) 1.18-1.35 (m, 8 H) 1.10 (d, J = 13.80 Hz, 4 H); HPLC: 96.8%, MS (ESI): 682.3 m/z [M + H]+
195		Yellow solid; 1H NMR (DMSO-d6, 400 MHz) δ 10.37 (1 H, s) 8.54 (1 H, d, J = 5.77 Hz) 8.48 (1 H, d, J = 1.76 Hz) 7.70-7.79 (3 H, m) 7.58-7.69 (3 H, m) 7.48 (2 H, dtd, J = 18.54, 7.42, 7.42, 1.51 Hz) 7.38 (1 H, dd, J = 7.53, 1.51 Hz) 6.47-6.56 (1 H, m) 6.31-6.40 (1 H, m) 5.82 (1 H, dd, J = 10.16, 1.88 Hz) 5.52 (1 H, s) 4.33 (2 H, d, J = 6.53 Hz) 2.21 (3 H, s) 1.27 (7 H, d, J = 6.78 Hz); LCMS: 100%, MS (ESI): m/z 477.1 [M + H]+
196		White solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 10.32 (1 H, br s) 8.36-8.56 (3 H, m) 8.14 (2 H, br s) 7.68 (1 H, d, J = 5.77 Hz) 7.61-7.65 (2 H, m) 7.52-7.60 (2 H, m) 7.40- 7.51 (2 H, m) 7.30-7.39 (2 H, m) 6.94 (2 H, br s) 6.26- 6.59 (4 H, m) 5.81 (1 H, dd, J = 10.16, 1.88 Hz) 4.38-4.53 (4 H, m) 2.63-2.73 (1 H, m) 2.52 (3 H, br s) 1.18-1.30 (6 H, m); LCMS: 100.0%, MS (ESI): m/z 590.1 [M + H]+
197		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.37 (1 H, s) 8.54 (1 H, d, J = 5.77 Hz) 8.46 (1 H, d, J = 1.51 Hz) 7.77 (1 H, d, J = 5.77 Hz) 7.54-7.75 (5 H, m) 7.43-7.53 (2 H, m) 7.33-7.40 (1 H, m) 6.45-6.56 (1 H, m) 6.29-6.39 (1 H, m) 5.81 (1 H, dd, J = 10.04, 1.76 Hz) 5.55 (1 H, s) 4.33 (2 H, br d, J = 6.02 Hz) 2.95-3.06 (1 H, m) 1.73 (1 H, quin, J = 6.40 Hz) 1.25 (6 H, d, J = 7.03 Hz) 0.86 (4 H, d, J = 6.53 Hz); HPLC: 98.32%, MS (ESI): m/z 503.1 [M + H]+
198		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.30 (6 H, d, J = 6.78 Hz) 3.15 (1 H, dt, J = 13.74, 7.06 Hz) 4.50 (2 H, br s) 5.79-5.83 (1 H, m) 6.12 (1 H, s) 6.31-6.37 (1 H, m) 6.46-6.55 (1 H, m) 7.37 (1 H, dd, J = 7.40, 1.38 Hz) 7.45-7.54 (3 H, m) 7.57-7.62 (1 H, m) 7.64 (1 H, d, J = 7.28 Hz) 7.71 (1 H, d, J = 5.77 Hz) 7.99 (1 H, s) 8.42 (1 H, d, J = 1.76 Hz) 8.49 (1 H, d, J = 5.77 Hz) 10.32 (1 H, s); HPLC: 99.78% MS (ESI): m/z 531.2 [M + H]+
199		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.37 (2 H, d, J = 5.2 Hz), 7.80 (1 H, s), 7.43-7.54 (1 H, m), 7.32-7.43 (2 H, m), 7.22 (1 H, dd, J = 8.0, 2.0 Hz), 7.17 (1 H, d, J = 4.0 Hz), 5.11-5.34 (2 H, m), 4.58-4.81 (3 H, m), 4.49 (2 H, br s), 3.61 (2 H, br s), 2.91-3.06 (2 H, m), 2.70- 2.81 (1 H, m), 2.57-2.63 (2 H, m), 1.91-2.09 (2 H, m), 1.63- 1.76 (1 H, m), 1.50-1.57 (1 H, m), 1.32-1.41 (1 H, m), 1.26 (6 H, d, J = 8.0 Hz), 1.07 (6 H, d, J = 12.0 Hz); HPLC (254 nm): 98.4%, MS (ESI): m/z 599.3 [M + H]+
200		White powder; 1H NMR (400 MHz, DMSO-d6) δ 9.27 (1 H, br s), 8.62 (1 H, br d, J = 8.0 Hz), 8.38 (1 H, br d, J = 8.0 Hz), 8.25-8.33 (2 H, m), 7.88 (1 H, br s), 7.67 (1 H, br d, J = 8.0 Hz), 7.44-7.55 (5 H, m), 7.32 (1 H, br d, J = 8.0 Hz), 6.45-6.52 (2 H, m), 6.27-6.35 (1 H, m), 5.75-5.85 (1 H, m), 2.85-2.95 (1 H, m), 4.65-4.76 (2 H, m) 1.33 (6 H, d, J = 8.0 Hz); HPLC: 98.8% (254 nm), MS (ESI): m/z 541.3 [M + H]+
201		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ 8.60- 8.72 (2 H, m), 8.39 (1 H, d, J = 4.0 Hz), 8.32 (1 H, d, J = 1.6 Hz), 7.88-7.98 (2 H, m), 7.67 (1 H, d, J = 8.0 Hz), 7.58-7.64 (1 H, m), 7.29-7.57 (6 H, m), 6.42-6.58 (1 H, m), 6.28-6.39 (1 H, m), 5.81 (1 H, dd, J = 12.0, 2.0 Hz), 5.14 (1 H, s), 5.11-5.19 (1 H, m), 4.65-4.76 (2 H, m), 3.25-3.33 (1 H, m), 2.91-2.99 (1 H, m), 1.34 (6 H, d, J = 8.0 Hz); HPLC: 97.6% (254 nm), MS (ESI): m/z 541.3 [M + H]+
202		White solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 10.35 (1 H, br s) 9.22 (1 H, br s) 8.45 (1 H, d, J = 5.77 Hz) 8.36 (1 H, s) 8.05 (1 H, s) 7.66 (1 H, d, J = 6.02 Hz) 7.55-7.62 (2 H, m) 7.44-7.54 (2 H, m) 7.30-7.40 (2 H, m) 6.84 (1 H, dt, J = 15.43, 6.46 Hz) 6.45 (1 H, s) 6.41 (1 H, s) 6.38-6.47 (1 H, m) 4.65 (2 H, br d, J = 14.56 Hz) 3.41-3.56 (2H, m) 3.13-3.14 (1 H, m) 3.14 (2H, s) 3.01-3.03 (2 H, m) 2.95- 3.03 (7 H, m) 1.29 (6 H, d, J = 6.78 Hz); LCMS: 97%, MS (ESI): m/z 599.1 [M + H]+
203		White powder; 1H NMR (400 MHz, DMSO-d6) δ 8.51 (1 H, br s), 8.37 (1 H, d, J = 4.0 Hz), 7.82 (1 H, s), 7.43-7.49 (1 H, m), 7.33-7.48 (1 H, m), 7.22 (1 H, br d, J = 12.0 Hz), 7.16 (1 H, d, J = 4.0 Hz), 6.70-6.85 (1 H, m), 6.12 (1 H, d, J = 16.0 Hz), 5.69 (1 H, br d, J = 8.0 Hz), 4.90 (1 H, br s), 4.67 (2 H, br s), 4.45-4.55 (2 H, m), 3.61 (2 H, br s), 2.99 (3 H, br d, J = 7.28 Hz), 1.95-2.05 (2 H, m), 1.77-1.82 (1 H, m), 1.58-1.68 (1 H. m), 1.42-1.54 (2 H, m), 1.12-1.30 (12 H, m); HPLC (254 nm): 98.8%, MS (ESI): m/z 581.4 [M + H]+
204		White powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.29 (5 H, d, J = 6.78 Hz) 2.22 (6 H, s) 2.93 (1 H, br s) 3.30 (2 H, br s) 4.49 (2 H, br s) 6.09 (1 H, s) 6.33 (1 H, br d, J = 15.31 Hz) 6.84 (1 H, dt, J = 15.37, 5.87 Hz) 7.35 (1 H, d, J = 7.28 Hz) 7.44-7.54 (3 H, m) 7.54-7.59 (1 H, m) 7.64 (1 H, d, J = 7.53 Hz) 7.69 (1 H, d, J = 5.52 Hz) 7.98 (1 H, s) 8.39 (1 H, s) 8.47 (1 H, d, J = 5.52 Hz) 10.24 (1 H, br s); LCMS: 95.92%, MS (ESI): m/z 588.3 [M + H]+
205		Yellow solid; 1H NMR (DMSO-d6, 400 MHz) δ 10.50 (1 H, s) 8.48-8.68 (2 H, m) 8.40 (2 H, s) 8.21 (1 H, s) 7.82 (1 H, d, J = 6.0 Hz) 7.76 (1 H, dd, J = 8.8, 2.4 Hz) 7.61 (3 H, t, J = 5.2 Hz) 7.54 (1 H, t, J = 7.2 Hz) 7.48 (1 H, t, J = 7.2 Hz) 7.38 (1 H, d, J = 7.6 Hz) 6.82 (1 H, d, J = 2.8 Hz) 6.36 (1 H, d, J = 3.2 Hz) 5.34 (1 H, t, J = 4.4 Hz) 4.49 (2 H, s) 3.54 (1 H, td, J = 9.2, 4.0 Hz) 3.43 (2 H, d, J = 14.4 Hz) 2.87-2.91 (1 H, m) 2.81 (1 H, s) 2.57 (1 H, s) 1.95-2.07 (2 H, m) 1.84 (1 H, d, J = 12.8 Hz) 1.71 (1 H, s) 1.40-1.52 (2 H, m) 1.26 (6 H, s); LCMS: 96.6%, MS (ESI): m/z 672.2 [M + H]+
206		Yellow solid; 1H NMR (DMSO-d6, 400 MHz) δ 10.46 (1 H, s) 8.61 (1 H, s) 8.51 (1 H, d, J = 6.0 Hz) 8.43 (2 H, d, J = 1.6 Hz) 7.75-7.87 (2 H, m) 7.62 (2 H, t, J = 4.2 Hz) 7.43-7.59 (2 H, m) 7.39 (1 H, d, J = 6.4 Hz) 6.51 (1 H, d, J = 2.4 Hz) 6.14 (1 H, d, J = 2.8 Hz) 4.50 (2 H, s) 3.51- 3.57 (1 H, m) 3.44 (1 H, d, J = 10.8 Hz) 3.26-3.35 (1 H, m) 3.24 (1 H, d, J = 10.8 Hz) 3.17 (1 H, d, J = 12.8 Hz) 2.85-2.92 (1 H, m) 2.81 (1 H, s) 1.94-2.12 (1H, m) 1.84 (1 H, d, J = 13.2 Hz) 1.69 (1 H, d, J = 10.8 Hz) 1.33-1.51 (1 H, m) 1.26 (1 H, s) 1.21 (6 H, d, J = 7.2 Hz); LCMS: 99.7%, MS (ESI): m/z 626.3 [M + H]+
207		White solid; 1H NMR (400 MHz, DMSO-d6) δ ppm 9.95 (1 H, br s) 9.02 (1 H, br d, J = 5.52 Hz) 8.90 (1 H, d, J = 2.26 Hz) 8.46 (1 H, d, J = 5.77 Hz) 8.39 (1 H, d, J = 1.76 Hz) 8.27 (1 H, br s) 8.11-8.19 (2 H, m) 7.71-7.79 (2 H, m) 7.66 (1 H, d, J = 5.77 Hz) 7.60 (2 H, d, J = 8.78 Hz) 7.43-7.54 (2 H, m) 7.36 (1 H, dd, J = 7.40, 1.38 Hz) 7.22 (1 H, dd, J = 8.41, 4.64 Hz) 5.88 (1 H, s) 5.57 (1 H, s) 4.57 (2 H, br d, J = 5.02 Hz) 2.99 (1 H, dt, J = 13.87, 7.00 Hz) 2.01 (3 H, s) 1.29 (6 H, d, J = 6.78 Hz); LCMS: 99%, MS (ESI): m/z 570.3 [M + H]+
208		Yellow powder; 1H NMR (DMSO-d6, 400 MHz) δ 9.97 (1 H, s) 8.48 (2 H, d, J = 5.6 Hz) 8.41 (1 H, s) 8.00 (1 H, s) 7.69-7.76 (2 H, m) 7.64 (1 H, d, J = 7.2 Hz) 7.44-7.54 (3 H, m) 7.34-7.38 (1H, m) 6.14 (1 H, s) 5.89 (1 H, s) 5.57 (1 H, s) 4.49 (2 H, s) 3.04-3.08 (1 H, m) 2.01 (3 H, s) 1.30 (6 H, d, J = 7.2 Hz); LCMS: 97.9%, MS (ESI): m/z 545.2 [M + H]+
209		White solid; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.38 (1 H, br s) 8.50 (1 H, d, J = 5.52 Hz) 8.40 (1 H, s) 7.93 (1 H, br s) 7.72-7.80 (2 H, m) 7.54-7.65 (3 H, m) 7.41-7.52 (2 H, m) 7.34 (1 H, d, J = 7.28 Hz) 6.49 (1 H, d, J = 2.51 Hz) 6.11 (1 H, d, J = 2.51 Hz) 5.91 (1 H, br s) 4.45 (2 H, br s) 3.55 (1 H, br s) 3.24 (3 H, s) 3.08 (1 H, br s) 2.88 (1 H, quin, J = 6.96 Hz) 1.83-2.01 (4 H, m) 1.25 (2 H, br d, J = 7.03 Hz) 1.21 (6 H, d, J = 6.78 Hz) 1.13-1.18 (2 H, m); LCMS: 100%, MS (ESI): m/z 625.1 [M + H]+
210		White powder; 1H NMR (400 MHz, DMSO-d6) δ 10.33 (1 H, br s), 8.47 (1 H, d, J = 5.6 Hz), 8.42 (1 H, s), 8.15 (1 H, br s), 7.71 (1 H, d, J = 5.6 Hz), 7.52-7.67 (3 H, m), 7.40- 7.51 (2 H, m), 7.32-7.37 (1 H, m), 6.45-6.59 (1 H, m), 6.26-6.42 (1 H, m), 5.76-5.88 (1 H, m), 4.46 (2 H, br s), 3.44-3.61 (4 H, m), 3.13-3.20 (2 H, m), 2.85-2.95 (1 H, m), 2.53-2.59 (4 H, m) 1.16-1.30 (6 H, m); HPLC (254 nm): 97.9%, MS (ESI): m/z 630.1 [M + H]+
211		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ 10.34 (1 H, br s), 8.40-8.55 (2 H, m), 8.11 (1 H, br s), 7.70 (1 H, d, J = 4.8 Hz), 7.41-7.64 (5 H, m), 7.31-7.37 (1 H, m), 6.46- 6.61 (1 H, m), 6.26-6.39 (1 H, m), 5.82 (1 H, dd, J = 10.0, 2.0 Hz), 4.48 (2 H, br s), 4.22-4.35 (1 H, m), 3.96 (1 H, d, J = 12.0 Hz), 3.22-3.35 (1 H, m), 2.83-2.96 (2 H, m), 2.53- 2.73 (3 H, m), 1.23 (6 H, d, J = 8.0 Hz); HPLC (254 nm): 98.2%, MS (ESI): m/z 616.3 [M + H]+
212		Yellow solid; 1H NMR (DMSO-d6, 400 MHz) δ 10.34 (1 H, s) 8.40-8.49 (2 H, m) 8.36 (1 H, d, J = 4.52 Hz) 8.14 (1 H, br s) 7.67 (1 H, d, J = 5.77 Hz) 7.59-7.63 (1 H, m) 7.53- 7.57 (1 H, m) 7.42-7.53 (3 H, m) 7.35 (1 H, d, J = 6.27 Hz) 7.19 (1 H, dd, J = 7.53, 4.77 Hz) 6.46-6.55 (1 H, m) 6.30- 6.37 (1 H, m) 5.81 (1 H, dd, J = 10.29, 1.51 Hz) 4.71 (2 H, s) 4.52 (2 H, s) 3.89 (2 H, t, J = 5.90 Hz) 2.94 (1 H, dt, J = 13.68, 6.71 Hz) 2.86 (2 H, t, J = 5.77 Hz) 1.25 (6 H, d, J = 6.78 Hz); LCMS: 97.7%, MS (ESI): m/z 596.4 [M + H]+
213		White powder; 1H NMR (400 MHz, DMSO-d6) δ 10.23 (1 H, s) 8.95 (1 H, s) 8.88 (1 H, d, J = 2.0 Hz) 8.29 (1 H, d, J = 5.6 Hz) 8.25 (1 H, s) 8.06-8.18 (2 H, m) 7.97 (1 H, d, J = 7.6 Hz) 7.83 (1 H, s) 7.70-7.76 (1 H, m) 7.63-7.68 (1 H, m) 7.58 (1 H, s) 7.45-7.55 (3 H, m) 7.24 (1 H, dd, J = 8.0, 4.4 Hz) 7.21-7.28 (1 H, m) 6.42-6.53 (1 H, m) 6.25- 6.36 (1 H, m) 5.79 (1 H, dd, J = 10.4, 1.6 Hz) 5.24 (1 H, d, J = 14.0 Hz) 4.26 (1 H, d, J = 14.4 Hz) 2.90 (1 H, m) 1.24 (6 H, d, J = 6.8 Hz); HPLC (254 nm): 98.2%, MS (ESI): m/z 624.2 [M + H]+
214		Yellow powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.46 (1 H, br s) 8.39-8.51 (2 H, m) 7.66-7.78 (2 H, m) 7.58-7.64 (2 H, m) 7.40-7.56 (4 H, m) 7.32-7.37 (1 H, m) 6.84 (1 H, dt, J = 15.43, 5.96 Hz) 6.40 (1 H, br d, J = 15.56 Hz) 5.34 (1 H, s) 4.26-4.34 (3 H, m) 3.76 (1 H, br d, J = 12.30 Hz) 3.27-3.39 (4 H, m) 2.92-3.05 (2 H, m) 2.66- 2.73 (2 H, m) 2.23 (6 H, s) 1.91-2.09 (1 H, m) 1.25 (6 H, d, J = 6.78 Hz); LCMS: 98.05%, MS (ESI): m/z 672.3 [M + H]+
215		Off-white powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.32 (1 H, br s) 8.47 (1 H, br d, J = 5.77 Hz) 8.41 (1 H, s) 7.92-8.05 (1 H, m) 7.62-7.77 (2 H, m) 7.58 (1 H, br d, J = 7.78 Hz) 7.41-7.54 (2 H, m) 7.35 (1 H, br d, J = 7.03 Hz) 6.50 (1 H, br dd, J = 16.94, 10.16 Hz) 6.33 (1 H, br dd, J = 17.07, 1.76 Hz) 5.75-5.86 (1 H, m) 4.50 (2 H, br s) 3.19 (3 H, br s) 3.04 (3 H, br s) 2.45 (2 H, br s) 1.94-2.10 (2 H, m) 1.49 (2 H, br s) 1.29-1.36 (1 H, m) 1.26 (3 H, s) 1.08 (3 H, s); LCMS: 100%, MS (ESI): m/z 616.4 [M + H]−
216		Off-white powder; 1H NMR (400 MHz, DMSO-d6) δ ppm 11.50 (br s, 1 H) 10.43 (br s, 1 H) 8.53 (br s, 1 H) 7.75 (br d, J = 8.28 Hz, 1 H) 7.71 (s, 1 H) 7.55-7.64 (m, 2 H) 7.37 (m, 3 H) 7.13 (br d, J = 3.51 Hz, 1 H) 7.01 (br t, J = 7.78 Hz, 1 H) 6.79-6.87 (m, 2 H) 6.71 (br d, J = 3.26 Hz, 1 H) 6.64 (d, J = 2.01 Hz, 1 H) 4.96 (br d, J = 6.53 Hz, 2 H) 4.25 (br s, 1 H) 3.95 (br d, J = 5.77 Hz, 2 H) 3.66 (br s, 1 H) 3.45-3.51 (m, 1 H) 3.40 (m, 2 H) 2.93-3.00 (m, 1 H) 2.82 (s, 6 H) 2.13 (m, 1 H) 1.89 (m, 1 H) 1.25 (d, J = 7.03 Hz, 6 H); HPLC: 96.6%, MS (ESI): 698.4 m/z [M + Na]+